A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620830



Internal ID7007700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79466422..79467680hg38UCSC Ensembl
Innerchr9:79466453..79467649hg38UCSC Ensembl
Outerchr9:79466391..79467711hg38UCSC Ensembl
chr9:82081337..82082595hg19UCSC Ensembl
Innerchr9:82081368..82082564hg19UCSC Ensembl
Outerchr9:82081306..82082626hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13534787, essv13534786, essv13534785, essv13534796, essv13534788, essv13534795, essv13534789, essv13534791, essv13534790, essv13534793, essv13534792, essv13534794
SamplesNA19703, HG03521, HG03298, HG03515, HG03572, HG03074, HG02620, NA19027, HG03136, NA19042, HG03162, NA18522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620830
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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