A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595445



Internal ID16382854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132101486..132417610hg38UCSC Ensembl
Innerchr4:133022641..133338765hg19UCSC Ensembl
Innerchr4:133242091..133558215hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38316125
hg19316125
hg18316125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1006514
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595445
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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