A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523783



Internal ID15451076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:96400344..96405703hg38UCSC Ensembl
Innerchr6:96848220..96853579hg19UCSC Ensembl
Innerchr6:96954941..96960300hg18UCSC Ensembl
Innerchr6:96954941..96960300hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385360
hg195360
hg185360
hg175360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699608
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523783
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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