A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595072



Internal ID16382481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107130343..107154557hg38UCSC Ensembl
Innerchr4:108051500..108075714hg19UCSC Ensembl
Innerchr4:108270949..108295163hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3824215
hg1924215
hg1824215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1004075
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595072
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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