A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694890



Internal ID15431542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27059034..27200330hg38UCSC Ensembl
Innerchr14:27528240..27669536hg19UCSC Ensembl
Innerchr14:26598080..26739376hg18UCSC Ensembl
Innerchr14:26598080..26739376hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38141297
hg19141297
hg18141297
hg17141297
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522117
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694890
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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