A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526130



Internal ID15453423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69141924..69212435hg38UCSC Ensembl
Innerchr6:69851816..69922327hg19UCSC Ensembl
Innerchr6:69908537..69979048hg18UCSC Ensembl
Innerchr6:69908537..69979048hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3870512
hg1970512
hg1870512
hg1770512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702384
Samples
Known GenesBAI3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526130
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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