A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517537



Internal ID15444830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154860892..154914071hg38UCSC Ensembl
Innerchr7:154652602..154705781hg19UCSC Ensembl
Innerchr7:154283535..154336714hg18UCSC Ensembl
Innerchr7:154090250..154143429hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3853180
hg1953180
hg1853180
hg1753180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653345, nssv665138, nssv652295, nssv674425, nssv683656, nssv654300, nssv694057, nssv692722, nssv658517, nssv675122, nssv661617, nssv693842, nssv684892
Samples
Known GenesDPP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517537
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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