A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631982



Internal ID7018792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46277412..46406201hg38UCSC Ensembl
chr13:46851547..46980336hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38128790
hg19128790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14713253
SamplesHG01850
Known GenesKIAA0226L, LINC00563
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631982
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