A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667300



Internal ID9933405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63015401..63015814hg38UCSC Ensembl
chr10:64775161..64775574hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6305816, essv5409053, essv6551796, essv5770597, essv6279964, essv5469900, essv5846326, essv6488425, essv5932884, essv6496403, essv5652077, essv6108026, essv6041700, essv6474796, essv5877769, essv5576566, essv5524033, essv6144062
SamplesNA19396, NA19379, NA18519, NA19382, NA19404, NA19371, NA19385, NA19901, NA18985, NA19445, HG01136, NA19707, NA18499, NA19469, NA19318, NA19401, NA19390, NA19434
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667300
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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