A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712304



Internal ID18663899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42709000..42808429hg38UCSC Ensembl
Innerchr14:43178203..43277632hg19UCSC Ensembl
Innerchr14:42247953..42347382hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3899430
hg1999430
hg1899430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038324
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)nssv3712304
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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