A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594069



Internal ID16381478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42704111..42710097hg38UCSC Ensembl
Innerchr4:42706128..42712114hg19UCSC Ensembl
Innerchr4:42400885..42406871hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg385987
hg195987
hg185987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv996706, nssv996705
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594069
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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