A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666772



Internal ID9932877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9853803..9855124hg38UCSC Ensembl
Outerchr3:9853646..9855277hg38UCSC Ensembl
Innerchr3:9895487..9896808hg19UCSC Ensembl
Outerchr3:9895330..9896961hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381632
hg191632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6313254, essv5397828, essv6166049, essv5841686, essv6164771, essv5430437, essv5632688, essv6520245, essv5864704, essv6415179, essv5783198
SamplesNA19700, NA19819, NA19684, NA19455, NA19236, NA19982, HG01137, HG01108, NA19818, NA19900, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666772
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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