A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517934



Internal ID15098541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132741777..132751511hg38UCSC Ensembl
Innerchr6:133062916..133072650hg19UCSC Ensembl
Innerchr6:133104609..133114343hg18UCSC Ensembl
Innerchr6:133104609..133114343hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg389735
hg199735
hg189735
hg179735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695346
Samples
Known GenesVNN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517934
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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