A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524631



Internal ID15451924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1959689..1967978hg38UCSC Ensembl
Innerchr8:1907855..1916144hg19UCSC Ensembl
Innerchr8:1895262..1903551hg18UCSC Ensembl
Innerchr8:1895262..1903551hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg388290
hg198290
hg188290
hg178290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700594
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524631
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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