A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703875



Internal ID15440527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146020457..146034910hg38UCSC Ensembl
Innerchr7:145717550..145732003hg19UCSC Ensembl
Innerchr7:145348483..145362936hg18UCSC Ensembl
Innerchr7:145155198..145169651hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3814454
hg1914454
hg1814454
hg1714454
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527435
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703875
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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