A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596287



Internal ID16383696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179687324..179694504hg38UCSC Ensembl
Innerchr4:180608477..180615657hg19UCSC Ensembl
Innerchr4:180845471..180852651hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg387181
hg197181
hg187181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017052
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596287
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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