A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4790n54



Internal ID22772685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101251057..101253446hg38UCSC Ensembl
chr15:101791262..101793651hg19UCSC Ensembl
chr15:99608785..99611174hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382390
hg192390
hg182390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570847, nsv570843, nsv570846, nsv570848, nsv570840, nsv570842, nsv570841
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4790n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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