A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593334



Internal ID16034057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1622987..1677699hg38UCSC Ensembl
Innerchr4:1624714..1679426hg19UCSC Ensembl
Innerchr4:1594673..1649224hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3854713
hg1954713
hg1854552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv988438
Samples
Known GenesFAM53A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593334
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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