A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825697



Internal ID16119653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35137894..35141070hg38UCSC Ensembl
Innerchr14:35607100..35610276hg19UCSC Ensembl
Innerchr14:34676851..34680027hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg383177
hg193177
hg183177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564303
Supporting Variants
Samples
Known GenesKIAA0391
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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