A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695516



Internal ID15432168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63450427..63463451hg38UCSC Ensembl
Innerchr4:64316145..64329169hg19UCSC Ensembl
Innerchr4:63998740..64011764hg18UCSC Ensembl
Innerchr4:64144911..64157935hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3813025
hg1913025
hg1813025
hg1713025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518103
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695516
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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