A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680740



Internal ID15070706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34465957hg38UCSC Ensembl
Innerchr15:34718594..34758158hg19UCSC Ensembl
Innerchr15:32505886..32545450hg18UCSC Ensembl
Innerchr15:32505886..32545450hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3839565
hg1939565
hg1839565
hg1739565
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)nssv680740
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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