A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631978



Internal ID7018788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46150994..46219563hg38UCSC Ensembl
Innerchr13:46150994..46219563hg38UCSC Ensembl
Outerchr13:46150494..46220063hg38UCSC Ensembl
chr13:46725129..46793698hg19UCSC Ensembl
Innerchr13:46725129..46793698hg19UCSC Ensembl
Outerchr13:46724629..46794198hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3868570
hg1968570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14713248
SamplesNA20902
Known GenesLCP1, LRRC63
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631978
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