A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711389



Internal ID19009670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98711806..98731044hg38UCSC Ensembl
Innerchr14:99178143..99197381hg19UCSC Ensembl
Innerchr14:98247896..98267134hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3819239
hg1919239
hg1819239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035747
Supporting Variants
Samples
Known GenesC14orf177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3711389
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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