A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4541n54



Internal ID22772436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54393265..54504394hg38UCSC Ensembl
chr15:54685463..54796592hg19UCSC Ensembl
chr15:52472755..52583884hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38111130
hg19111130
hg18111130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569506, nsv569502, nsv569504, nsv569501
SamplesHGDP00592
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4541n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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