A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596280



Internal ID16383689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178744216..179151523hg38UCSC Ensembl
Innerchr4:179665370..180072677hg19UCSC Ensembl
Innerchr4:179902364..180309671hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38407308
hg19407308
hg18407308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153261
Samples1780854302_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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