A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527435



Internal ID15454728
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703875
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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