A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520074



Internal ID15447367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99860886..99863823hg38UCSC Ensembl
Innerchr4:100782043..100784980hg19UCSC Ensembl
Innerchr4:101001066..101004003hg18UCSC Ensembl
Innerchr4:101139221..101142158hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382938
hg192938
hg182938
hg172938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691558, nssv660543, nssv691192, nssv690348, nssv660495
Samples
Known GenesDAPP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520074
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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