A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519202



Internal ID15099809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:84168097..84173488hg38UCSC Ensembl
Innerchr6:84877816..84883207hg19UCSC Ensembl
Innerchr6:84934535..84939926hg18UCSC Ensembl
Innerchr6:84934535..84939926hg17UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg385392
hg195392
hg185392
hg175392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696687
Samples
Known GenesKIAA1009
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519202
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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