A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036406



Internal ID19125625
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 StatusM
Merged Variants
Supporting Variantsnssv3545673, nssv3721479
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)nsv1036406
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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