A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662962



Internal ID15399614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93599401..93619013hg38UCSC Ensembl
Innerchr15:94142630..94162242hg19UCSC Ensembl
Innerchr15:91943634..91963246hg18UCSC Ensembl
Innerchr15:91943634..91963246hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3819613
hg1919613
hg1819613
hg1719613
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515866
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer