A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713490



Internal ID19011771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48319210..48447768hg38UCSC Ensembl
Innerchr14:48788413..48916971hg19UCSC Ensembl
Innerchr14:47858163..47986721hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38128559
hg19128559
hg18128559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043059
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)nssv3713490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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