A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595746



Internal ID16383155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152982614..153002858hg38UCSC Ensembl
Innerchr4:153903766..153924010hg19UCSC Ensembl
Innerchr4:154123216..154143460hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3820245
hg1920245
hg1820245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009625
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595746
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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