A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524774



Internal ID15452067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153534660..154010300hg38UCSC Ensembl
Innerchr7:153231745..153707385hg19UCSC Ensembl
Innerchr7:152862678..153338318hg18UCSC Ensembl
Innerchr7:152669393..153145033hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38475641
hg19475641
hg18475641
hg17475641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700765
Samples
Known GenesDPP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524774
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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