A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520265



Internal ID15447558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20183522..20186124hg38UCSC Ensembl
Innerchr7:20223145..20225747hg19UCSC Ensembl
Innerchr7:20189670..20192272hg18UCSC Ensembl
Innerchr7:19996385..19998987hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382603
hg192603
hg182603
hg172603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681385, nssv689791, nssv662258, nssv683352
Samples
Known GenesMACC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520265
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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