A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521325



Internal ID15448618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117450980..117455022hg38UCSC Ensembl
Innerchr6:117772143..117776185hg19UCSC Ensembl
Innerchr6:117878836..117882878hg18UCSC Ensembl
Innerchr6:117878836..117882878hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg384043
hg194043
hg184043
hg174043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697931
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521325
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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