A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523539



Internal ID15450832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:82598745..82600109hg38UCSC Ensembl
Innerchr4:83519898..83521262hg19UCSC Ensembl
Innerchr4:83738922..83740286hg18UCSC Ensembl
Innerchr4:83877077..83878441hg17UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg381365
hg191365
hg181365
hg171365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699316
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523539
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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