A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528106



Internal ID15455399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68872099..68900389hg38UCSC Ensembl
Innerchr6:69581991..69610281hg19UCSC Ensembl
Innerchr6:69638712..69667002hg18UCSC Ensembl
Innerchr6:69638712..69667002hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3828291
hg1928291
hg1828291
hg1728291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704647
Samples
Known GenesBAI3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528106
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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