A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721476



Internal ID19019757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28713634hg38UCSC Ensembl
Innerchr15:28911758..28958780hg19UCSC Ensembl
Innerchr15:26710799..26757821hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3847023
hg1947023
hg1847023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036106
Supporting Variants
Samples
Known GenesGOLGA8M, HERC2P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721476
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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