A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669577



Internal ID15406229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68604047..68610740hg38UCSC Ensembl
Innerchr14:69070764..69077457hg19UCSC Ensembl
Innerchr14:68140517..68147210hg18UCSC Ensembl
Innerchr14:68140517..68147210hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg386694
hg196694
hg186694
hg176694
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516614
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669577
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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