A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594568



Internal ID16035291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68581133..68631558hg38UCSC Ensembl
Innerchr4:69446851..69497276hg19UCSC Ensembl
Innerchr4:69129446..69179871hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3850426
hg1950426
hg1850426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9110n54
Supporting Variantsnssv992750
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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