A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712291



Internal ID19010572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39947641..40120906hg38UCSC Ensembl
Innerchr14:40416845..40590110hg19UCSC Ensembl
Innerchr14:39486596..39659861hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38173266
hg19173266
hg18173266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043280
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)nssv3712291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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