A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688878



Internal ID15425530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26614451..26620276hg38UCSC Ensembl
Innerchr14:27083657..27089482hg19UCSC Ensembl
Innerchr14:26153497..26159322hg18UCSC Ensembl
Innerchr14:26153497..26159322hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385826
hg195826
hg185826
hg175826
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516289
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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