A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8903n54



Internal ID20142327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1870601..1872396hg38UCSC Ensembl
chr4:1872328..1874123hg19UCSC Ensembl
chr4:1842126..1843921hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381796
hg191796
hg181796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593344, nsv593359, nsv593352, nsv593345, nsv593351, nsv593353, nsv593358, nsv593342, nsv593341
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8903n54
Frequency
Sample Size17421
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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