A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832731



Internal ID15780001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96631316..96671344hg38UCSC Ensembl
Innerchr14:97097653..97137681hg19UCSC Ensembl
Innerchr14:96167406..96207434hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3840029
hg1940029
hg1840029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565651
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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