A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521668



Internal ID15448961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84556843..84716710hg38UCSC Ensembl
Innerchr7:84186159..84346026hg19UCSC Ensembl
Innerchr7:84024095..84183962hg18UCSC Ensembl
Innerchr7:83830810..83990677hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38159868
hg19159868
hg18159868
hg17159868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv422n21
Supporting Variantsnssv694471
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521668
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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