A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519350



Internal ID15446643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:97794165..97815737hg38UCSC Ensembl
Innerchr6:98242041..98263613hg19UCSC Ensembl
Innerchr6:98348762..98370334hg18UCSC Ensembl
Innerchr6:98348762..98370334hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3821573
hg1921573
hg1821573
hg1721573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692766, nssv655532
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519350
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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