A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4426n54



Internal ID18996602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30637055..30675803hg38UCSC Ensembl
chr15:30929258..30968006hg19UCSC Ensembl
chr15:28716550..28755298hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3838749
hg1938749
hg1838749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568756, nsv568755
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4426n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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