A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594057



Internal ID16381466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42695536..42706471hg38UCSC Ensembl
Innerchr4:42697553..42708488hg19UCSC Ensembl
Innerchr4:42392310..42403245hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3810936
hg1910936
hg1810936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9024n54
Supporting Variantsnssv996677
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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