A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712276



Internal ID19010557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33140899..33202974hg38UCSC Ensembl
Innerchr14:33610105..33672180hg19UCSC Ensembl
Innerchr14:32679856..32741931hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3862076
hg1962076
hg1862076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036028
Supporting Variants
Samples
Known GenesNPAS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712276
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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