A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523345



Internal ID15450638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:105544042..105547673hg38UCSC Ensembl
Innerchr6:105991917..105995548hg19UCSC Ensembl
Innerchr6:106098610..106102241hg18UCSC Ensembl
Innerchr6:106098610..106102241hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383632
hg193632
hg183632
hg173632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699094
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523345
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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