A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9098n54



Internal ID22776993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65718188..65773098hg38UCSC Ensembl
chr4:66583906..66638816hg19UCSC Ensembl
chr4:66266501..66321411hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3854911
hg1954911
hg1854911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594483, nsv594485, nsv594482, nsv594484, nsv594487, nsv594481, nsv594486
SamplesHGDP00537, HGDP01403, NINDS_240, HGDP01368, HGDP00538, 1780862517_A, 1780862373_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9098n54
Frequency
Sample Size17421
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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