A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528285



Internal ID15455578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29599065..29620369hg38UCSC Ensembl
Innerchr6:29566842..29588146hg19UCSC Ensembl
Innerchr6:29674821..29696125hg18UCSC Ensembl
Innerchr6:29674821..29696125hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3821305
hg1921305
hg1821305
hg1721305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704855
Samples
Known GenesGABBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528285
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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