A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531012



Internal ID18829293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48772389..49048066hg38UCSC Ensembl
Innerchr14:49241592..49514784hg19UCSC Ensembl
Innerchr14:48311342..48584534hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38275678
hg19273193
hg18273193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052323
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)nssv3531012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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