A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565443



Internal ID16352852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85821003..85871268hg38UCSC Ensembl
Innerchr14:86287347..86337612hg19UCSC Ensembl
Innerchr14:85357100..85407365hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850266
hg1950266
hg1850266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3828n54
Supporting Variantsnssv1149507, nssv1149508, nssv1149506, nssv831991
Samples1798860114_A, 1780862401_A, 1780862379_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565443
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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