A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721475



Internal ID19019756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28708757hg38UCSC Ensembl
Innerchr15:28911758..28953903hg19UCSC Ensembl
Innerchr15:26710799..26752944hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3842146
hg1942146
hg1842146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051351
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)nssv3721475
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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