A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565432



Internal ID16352841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85816380..85844001hg38UCSC Ensembl
Innerchr14:86282724..86310345hg19UCSC Ensembl
Innerchr14:85352477..85380098hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3827622
hg1927622
hg1827622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3825n54
Supporting Variantsnssv831946
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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