A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674426



Internal ID15064392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24262601..24272675hg38UCSC Ensembl
Innerchr7:24302220..24312294hg19UCSC Ensembl
Innerchr7:24268745..24278819hg18UCSC Ensembl
Innerchr7:24075460..24085534hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3810075
hg1910075
hg1810075
hg1710075
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517053
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674426
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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