A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665803



Internal ID9931908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88957210..88957345hg38UCSC Ensembl
chr3:89006360..89006495hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6037759, essv6436178, essv5424148, essv6582680, essv5920870, essv5686536, essv6166312, essv5472258, essv6361263, essv6033590, essv5816270, essv5954022, essv6388200, essv6476758, essv6379148, essv5971582, essv6377671, essv5612785, essv5924223, essv5858749, essv5949548, essv5931910, essv6162077, essv6559353, essv6212135, essv5807685, essv5552039, essv6184044, essv5965913, essv6379185, essv5484059, essv6505608, essv5613497, essv6527954, essv5443661, essv6444555, essv5759642, essv5807079, essv6531643, essv6217862, essv6265150, essv6224238, essv6084721, essv6179643, essv6561020, essv6180537
SamplesHG00650, HG00608, NA18861, NA18592, NA18980, NA18486, NA18504, HG00150, NA19373, NA20796, NA18618, NA20287, HG00427, NA19707, NA19070, HG00557, HG00577, HG00701, NA19391, HG00584, HG01498, HG00619, HG01073, NA19000, NA18532, HG00525, NA19059, NA19452, NA19682, NA18523, NA19395, NA18576, NA18546, NA19401, NA18909, HG00580, NA20530, NA19467, HG00418, HG00478, NA20758, NA18623, HG00554, NA18549, HG00437, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665803
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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