A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677020



Internal ID15066986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34451062hg38UCSC Ensembl
Innerchr15:34718594..34743263hg19UCSC Ensembl
Innerchr15:32505886..32530555hg18UCSC Ensembl
Innerchr15:32505886..32530555hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3824670
hg1924670
hg1824670
hg1724670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677020
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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