A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4376n54



Internal ID22772271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24821213..24869979hg38UCSC Ensembl
chr15:25066360..25115126hg19UCSC Ensembl
chr15:22617453..22666219hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3848767
hg1948767
hg1848767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568531, nsv568532
Samples1780862101_A
Known GenesSNRPN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4376n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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