A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671088



Internal ID9937193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89914318..89914682hg38UCSC Ensembl
Outerchr16:89914260..89914745hg38UCSC Ensembl
Innerchr16:89980726..89981090hg19UCSC Ensembl
Outerchr16:89980668..89981153hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv518e199
Supporting Variantsessv6351738, essv6265648, essv6086259, essv6568768, essv6327361, essv6359841, essv5562207, essv6452556, essv6570693, essv6499128, essv6154429, essv5910706, essv5533465, essv5831096, essv5665754, essv6381684, essv6081342, essv5561758, essv5530025, essv6248562, essv5768343, essv6437809, essv6574007, essv6494602, essv5763282, essv6521661, essv6437155, essv6393898, essv5707749, essv6287415, essv6595465, essv5510556, essv6228078, essv5577558, essv6474579, essv5580189, essv6489944, essv5462836, essv5469545, essv6480931, essv5778324, essv6128303, essv6125780, essv5583222, essv5737200, essv5448320, essv6190394, essv6294031, essv6443594, essv5912026, essv6340939, essv6083555, essv5707111, essv6255105, essv6417416, essv6277515, essv5871541, essv5734013, essv5718011, essv5464286, essv5981718, essv5448505, essv5702407, essv6582418, essv6167407, essv5958955, essv6056920, essv5858865, essv5454085, essv6269449, essv5742635, essv5872800, essv6525489, essv6104985, essv6259453, essv6371093, essv6122201, essv6100668, essv6176998, essv6435953, essv5486159, essv5395770, essv5565461, essv6543891, essv5487396, essv5747712, essv6006665
SamplesNA19394, NA12383, HG00442, NA19700, NA19055, HG00231, HG01389, HG01374, HG00151, HG00699, NA19819, NA19377, NA18959, NA18616, HG00654, NA19446, NA19005, HG00702, NA18567, NA20769, HG00270, HG00185, HG00537, HG01134, NA20759, HG01067, NA18617, NA19471, HG01440, NA19002, HG01198, HG01048, NA19445, NA19921, HG00739, HG00464, HG01136, NA18613, HG00731, HG00380, NA19077, NA19462, HG00190, HG00701, NA19236, NA19982, HG00583, NA12718, NA20126, NA19654, NA19000, NA19084, HG00157, NA19009, NA18963, NA19318, NA19685, NA18953, NA19729, NA19440, NA12716, NA19473, NA18628, NA19010, HG01375, NA19835, HG00607, NA19467, NA20516, HG01108, NA18615, NA19818, NA19078, HG00614, NA19060, HG00656, HG00342, NA20334, NA19716, NA19102, HG00698, NA20758, NA19780, NA18989, NA19004, HG01061, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671088
Frequency
Sample Size1151
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


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