A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526720



Internal ID15454013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154168113..154249466hg38UCSC Ensembl
Innerchr7:153865198..153946551hg19UCSC Ensembl
Innerchr7:153496131..153577484hg18UCSC Ensembl
Innerchr7:153302846..153384199hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3881354
hg1981354
hg1881354
hg1781354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703060
Samples
Known GenesDPP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526720
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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