A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594070



Internal ID16381479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42704594..42706908hg38UCSC Ensembl
Innerchr4:42706611..42708925hg19UCSC Ensembl
Innerchr4:42401368..42403682hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382315
hg192315
hg182315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9025n54
Supporting Variantsnssv996707
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594070
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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