A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595506



Internal ID16382915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134567613..134626139hg38UCSC Ensembl
Innerchr4:135488768..135547294hg19UCSC Ensembl
Innerchr4:135708218..135766744hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3858527
hg1958527
hg1858527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1007624
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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