A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4624n54



Internal ID22772519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74417064..74418781hg38UCSC Ensembl
chr15:74709405..74711122hg19UCSC Ensembl
chr15:72496458..72498175hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381718
hg191718
hg181718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569978, nsv569977
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4624n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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