A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520873



Internal ID15448166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85114605..85124486hg38UCSC Ensembl
Innerchr6:85824323..85834204hg19UCSC Ensembl
Innerchr6:85881042..85890923hg18UCSC Ensembl
Innerchr6:85881042..85890923hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg389882
hg199882
hg189882
hg179882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678561, nssv676670, nssv703729
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520873
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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