A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527544



Internal ID15454837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:115077995..115339774hg38UCSC Ensembl
Innerchr6:115399159..115660938hg19UCSC Ensembl
Innerchr6:115505852..115767631hg18UCSC Ensembl
Innerchr6:115505852..115767631hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38261780
hg19261780
hg18261780
hg17261780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704005
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527544
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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