A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712297



Internal ID19010578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41378051..41491211hg38UCSC Ensembl
Innerchr14:41847254..41960414hg19UCSC Ensembl
Innerchr14:40917004..41030164hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38113161
hg19113161
hg18113161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044555
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)nssv3712297
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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