A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829523



Internal ID16123479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75053362..75057829hg38UCSC Ensembl
Innerchr14:75520065..75524532hg19UCSC Ensembl
Innerchr14:74589818..74594285hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384468
hg194468
hg184468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565189
Supporting Variants
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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