A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521891



Internal ID15102498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115061920..115074228hg38UCSC Ensembl
Innerchr7:114701974..114714282hg19UCSC Ensembl
Innerchr7:114489210..114501518hg18UCSC Ensembl
Innerchr7:114295925..114308233hg17UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3812309
hg1912309
hg1812309
hg1712309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694663
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521891
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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