A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705106



Internal ID15441758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35356230..35371472hg38UCSC Ensembl
Innerchr14:35825436..35840678hg19UCSC Ensembl
Innerchr14:34895187..34910429hg18UCSC Ensembl
Innerchr14:34895187..34910429hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3815243
hg1915243
hg1815243
hg1715243
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528501
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705106
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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