A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545673



Internal ID18843954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28768018hg38UCSC Ensembl
Innerchr15:28911758..29013164hg19UCSC Ensembl
Innerchr15:26710799..26812205hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38101407
hg19101407
hg18101407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036406
Supporting Variants
Samples
Known GenesGOLGA8M, HERC2P9, WHAMMP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545673
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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