A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515997



Internal ID15443054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89905292..90253815hg38UCSC Ensembl
Innerchr7:89534606..89883129hg19UCSC Ensembl
Innerchr7:89372542..89721065hg18UCSC Ensembl
Innerchr7:89179257..89527780hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38348524
hg19348524
hg18348524
hg17348524
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700692, nssv677432, nssv695806, nssv702277, nssv665639, nssv697020, nssv657361
Samples
Known GenesC7orf63, DPY19L2P4, STEAP1, STEAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515997
Frequency
Sample Size2026
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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