A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565434



Internal ID16352843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85816380..85845829hg38UCSC Ensembl
Innerchr14:86282724..86312173hg19UCSC Ensembl
Innerchr14:85352477..85381926hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3829450
hg1929450
hg1829450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3825n54
Supporting Variantsnssv831948, nssv831951, nssv831949, nssv831950
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565434
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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