A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521802



Internal ID15449095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169797705..169806629hg38UCSC Ensembl
Innerchr6:170197801..170206725hg19UCSC Ensembl
Innerchr6:169939726..169948650hg18UCSC Ensembl
Innerchr6:170015433..170024357hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388925
hg198925
hg188925
hg178925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694572
Samples
Known GenesLINC00242, LINC00574
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521802
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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