A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521089



Internal ID15448382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43375407..43384513hg38UCSC Ensembl
Innerchr7:43415006..43424112hg19UCSC Ensembl
Innerchr7:43381531..43390637hg18UCSC Ensembl
Innerchr7:43188246..43197352hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg389107
hg199107
hg189107
hg179107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681774, nssv689106, nssv687061
Samples
Known GenesHECW1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521089
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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