A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690996



Internal ID15080962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34496365hg38UCSC Ensembl
Innerchr15:34718594..34788566hg19UCSC Ensembl
Innerchr15:32505886..32575858hg18UCSC Ensembl
Innerchr15:32505886..32575858hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3869973
hg1969973
hg1869973
hg1769973
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv690996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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