A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565577



Internal ID16352986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93987862..93988487hg38UCSC Ensembl
Innerchr14:94454208..94454833hg19UCSC Ensembl
Innerchr14:93523961..93524586hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38626
hg19626
hg18626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3853n54
Supporting Variantsnssv832437
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565577
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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