A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518455



Internal ID15445748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73978273..74001838hg38UCSC Ensembl
Innerchr7:73392603..73416168hg19UCSC Ensembl
Innerchr7:73030539..73054104hg18UCSC Ensembl
Innerchr7:72837254..72860819hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3823566
hg1923566
hg1823566
hg1723566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695891
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518455
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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