A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825728



Internal ID16119684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35533726..35534655hg38UCSC Ensembl
Innerchr14:36002932..36003861hg19UCSC Ensembl
Innerchr14:35072683..35073612hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38930
hg19930
hg18930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564321
Supporting Variants
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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