A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721474



Internal ID19019755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28697547hg38UCSC Ensembl
Innerchr15:28911758..28942693hg19UCSC Ensembl
Innerchr15:26710799..26741734hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3830936
hg1930936
hg1830936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043741
Supporting Variants
Samples
Known GenesHERC2P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721474
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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