A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565425



Internal ID16352834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85099643..85150459hg38UCSC Ensembl
Innerchr14:85565987..85616803hg19UCSC Ensembl
Innerchr14:84635740..84686556hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850817
hg1950817
hg1850817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831939
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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