A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565428



Internal ID16352837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85687683..85900036hg38UCSC Ensembl
Innerchr14:86154027..86366380hg19UCSC Ensembl
Innerchr14:85223780..85436133hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38212354
hg19212354
hg18212354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831941
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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