A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522858



Internal ID15450151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85841267..85869115hg38UCSC Ensembl
Innerchr6:86550985..86578833hg19UCSC Ensembl
Innerchr6:86607704..86635552hg18UCSC Ensembl
Innerchr6:86607704..86635552hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3827849
hg1927849
hg1827849
hg1727849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698513
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522858
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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