A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526385



Internal ID15453678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9523961..9529786hg38UCSC Ensembl
Innerchr6:9524194..9530019hg19UCSC Ensembl
Innerchr6:9632180..9638005hg18UCSC Ensembl
Innerchr6:9632180..9638005hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg385826
hg195826
hg185826
hg175826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702683
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526385
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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