A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703864



Internal ID15440516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27490199..27554600hg38UCSC Ensembl
Innerchr14:27959405..28023806hg19UCSC Ensembl
Innerchr14:27029245..27093646hg18UCSC Ensembl
Innerchr14:27029245..27093646hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3864402
hg1964402
hg1864402
hg1764402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520836
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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