A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517991



Internal ID15445284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16002971..16064702hg38UCSC Ensembl
Innerchr7:16042596..16104327hg19UCSC Ensembl
Innerchr7:16009121..16070852hg18UCSC Ensembl
Innerchr7:15815836..15877567hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3861732
hg1961732
hg1861732
hg1761732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695404
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517991
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer