A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4623n54



Internal ID20138047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74416730..74419428hg38UCSC Ensembl
chr15:74709071..74711769hg19UCSC Ensembl
chr15:72496124..72498822hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569980, nsv569981, nsv569975
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4623n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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