A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4601n54



Internal ID22772496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71586714..71590286hg38UCSC Ensembl
chr15:71879053..71882625hg19UCSC Ensembl
chr15:69666107..69669679hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383573
hg193573
hg183573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569880, nsv569881
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4601n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer