A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526756



Internal ID15107363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158918188..159326796hg38UCSC Ensembl
Innerchr7:158710879..159119486hg19UCSC Ensembl
Innerchr7:158403640..158812247hg18UCSC Ensembl
Innerchr7:158210355..158618962hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38408609
hg19408608
hg18408608
hg17408608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703106
Samples
Known GenesLINC00689, VIPR2, WDR60
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526756
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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