A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4625n54



Internal ID22772520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74426687..74429720hg38UCSC Ensembl
chr15:74719028..74722061hg19UCSC Ensembl
chr15:72506081..72509114hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383034
hg193034
hg183034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569984, nsv569983, nsv569985
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4625n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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