A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691597



Internal ID15081563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44802081hg38UCSC Ensembl
Innerchr10:45210690..45297529hg19UCSC Ensembl
Innerchr10:44530696..44617535hg18UCSC Ensembl
Innerchr10:44530696..44617535hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3886840
hg1986840
hg1886840
hg1786840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517161
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691597
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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