A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825149



Internal ID16119105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33086348..33122008hg38UCSC Ensembl
Innerchr14:33555554..33591214hg19UCSC Ensembl
Innerchr14:32625305..32660965hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3835661
hg1935661
hg1835661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564186
Supporting Variants
Samples
Known GenesNPAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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