A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695637



Internal ID15085603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34360482..34508394hg38UCSC Ensembl
Innerchr15:34652683..34800595hg19UCSC Ensembl
Innerchr15:32439975..32587887hg18UCSC Ensembl
Innerchr15:32439975..32587887hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38147913
hg19147913
hg18147913
hg17147913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known GenesGOLGA8A, LPCAT4, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695637
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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