A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713485



Internal ID19011766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47801072..47893881hg38UCSC Ensembl
Innerchr14:48270275..48363084hg19UCSC Ensembl
Innerchr14:47340025..47432834hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3892810
hg1992810
hg1892810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038432
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)nssv3713485
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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