A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678367



Internal ID15415019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38489763..38564099hg38UCSC Ensembl
Innerchr14:38958967..39033303hg19UCSC Ensembl
Innerchr14:38028718..38103054hg18UCSC Ensembl
Innerchr14:38028718..38103054hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3874337
hg1974337
hg1874337
hg1774337
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515869
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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