A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524559



Internal ID15105166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123189871..124008531hg38UCSC Ensembl
Innerchr6:123511016..124329676hg19UCSC Ensembl
Innerchr6:123552715..124371375hg18UCSC Ensembl
Innerchr6:123552715..124371375hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38818661
hg19818661
hg18818661
hg17818661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700513
Samples
Known GenesNKAIN2, TRDN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524559
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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