A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526829



Internal ID15454122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89411272..89417671hg38UCSC Ensembl
Innerchr6:90120991..90127390hg19UCSC Ensembl
Innerchr6:90177710..90184109hg18UCSC Ensembl
Innerchr6:90177710..90184109hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg386400
hg196400
hg186400
hg176400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703186
Samples
Known GenesRRAGD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526829
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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