A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693257



Internal ID15429909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97644001..97644081hg38UCSC Ensembl
Innerchr14:98110338..98110418hg19UCSC Ensembl
Innerchr14:97180091..97180171hg18UCSC Ensembl
Innerchr14:97180091..97180171hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3881
hg1981
hg1881
hg1781
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521281
Supporting Variants
Samples
Known GenesLOC100129345
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693257
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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