A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721630



Internal ID19019911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179274..32283629hg38UCSC Ensembl
Innerchr15:32471475..32575830hg19UCSC Ensembl
Innerchr15:30258767..30363122hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38104356
hg19104356
hg18104356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045626
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721630
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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