A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515820



Internal ID15442877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135673698..135739111hg38UCSC Ensembl
Innerchr3:135392540..135457953hg19UCSC Ensembl
Innerchr3:136875230..136940643hg18UCSC Ensembl
Innerchr3:136875238..136940651hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3865414
hg1965414
hg1865414
hg1765414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664876, nssv684624, nssv679173, nssv693764, nssv678123, nssv654629, nssv656574, nssv679979, nssv658995, nssv661764, nssv655970, nssv658541, nssv691160, nssv668817, nssv680017, nssv677027, nssv674126, nssv686781, nssv656546
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515820
Frequency
Sample Size2026
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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