A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594698



Internal ID16382107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77370722..77413329hg38UCSC Ensembl
Innerchr4:78291876..78334483hg19UCSC Ensembl
Innerchr4:78510900..78553507hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3842608
hg1942608
hg1842608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1002372
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594698
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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