A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713491



Internal ID19011772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48319210..48450204hg38UCSC Ensembl
Innerchr14:48788413..48919407hg19UCSC Ensembl
Innerchr14:47858163..47989157hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38130995
hg19130995
hg18130995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046630
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)nssv3713491
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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