A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518835



Internal ID15446128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139448930..139479755hg38UCSC Ensembl
Innerchr6:139770067..139800892hg19UCSC Ensembl
Innerchr6:139811760..139842585hg18UCSC Ensembl
Innerchr6:139811760..139842585hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3830826
hg1930826
hg1830826
hg1730826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696288
Samples
Known GenesLOC645434
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518835
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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