A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636436



Internal ID6676543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50098710..50166942hg38UCSC Ensembl
chr15:50390907..50459139hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3868233
hg1968233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15246635
SamplesHG04153
Known GenesATP8B4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636436
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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