A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595577



Internal ID16382986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137931922..137981717hg38UCSC Ensembl
Innerchr4:138853076..138902871hg19UCSC Ensembl
Innerchr4:139072526..139122321hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3849796
hg1949796
hg1849796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1007953
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595577
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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