A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664937



Internal ID9931042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165045815..165046589hg38UCSC Ensembl
chr4:165966967..165967741hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5946336, essv6468739, essv5799250, essv5803867, essv6146603, essv5876619, essv5568837, essv6414451, essv6316156, essv5594292, essv5425035, essv6003042, essv6306368, essv5788113, essv5829192, essv5616464, essv6437151, essv6190681, essv5547249, essv6496512, essv6194847, essv6417478, essv5639658, essv6236179, essv5979228, essv5557130, essv5464365, essv5823361, essv5969609, essv5480225, essv5592180, essv5772454, essv6299470, essv5519192, essv6215345, essv5954690, essv5741471, essv6280111, essv5802083, essv6076332
SamplesNA11995, NA18861, NA18507, NA19092, NA18870, NA19920, NA19107, NA07346, NA19396, NA18519, NA19198, NA18916, NA19384, NA18874, NA19238, NA19172, NA19159, NA19209, NA19985, NA11831, NA19210, NA19152, NA18516, NA18871, NA18856, NA12892, NA18853, NA19257, NA19225, NA19395, NA18909, NA11881, NA19144, NA19835, NA18943, NA19472, NA19713, NA19474, NA19093, NA19116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664937
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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