A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528634



Internal ID18826915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38325222..38343186hg38UCSC Ensembl
Innerchr14:38794426..38812390hg19UCSC Ensembl
Innerchr14:37864177..37882141hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3817965
hg1917965
hg1817965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054423
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)nssv3528634
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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