A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594097



Internal ID16381506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44463853..44534337hg38UCSC Ensembl
Innerchr4:44465870..44536354hg19UCSC Ensembl
Innerchr4:44160627..44231111hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3870485
hg1970485
hg1870485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152676
Samples1780854202_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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