A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565455



Internal ID16352864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85983020..86020992hg38UCSC Ensembl
Innerchr14:86449364..86487336hg19UCSC Ensembl
Innerchr14:85519117..85557089hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3837973
hg1937973
hg1837973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3832n54
Supporting Variantsnssv832011, nssv1149510
SamplesNINDS_96
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565455
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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