A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522536



Internal ID15449829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135308242..135398492hg38UCSC Ensembl
Innerchr4:136229397..136319647hg19UCSC Ensembl
Innerchr4:136448847..136539097hg18UCSC Ensembl
Innerchr4:136587002..136677252hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3890251
hg1990251
hg1890251
hg1790251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705910
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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