A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523840



Internal ID15451133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:61408908..61423314hg38UCSC Ensembl
Innerchr4:62274626..62289032hg19UCSC Ensembl
Innerchr4:61957221..61971627hg18UCSC Ensembl
Innerchr4:62103392..62117798hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3814407
hg1914407
hg1814407
hg1714407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699672
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523840
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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