A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595332



Internal ID16036055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119237579..119259635hg38UCSC Ensembl
Innerchr4:120158734..120180790hg19UCSC Ensembl
Innerchr4:120378182..120400238hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3822057
hg1922057
hg1822057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1006067, nssv1006068
Samples
Known GenesUSP53
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595332
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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