A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593341



Internal ID16034064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870601..1871959hg38UCSC Ensembl
Innerchr4:1872328..1873686hg19UCSC Ensembl
Innerchr4:1842126..1843484hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381359
hg191359
hg181359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8903n54
Supporting Variantsnssv988445
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593341
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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