A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631810



Internal ID7018619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37851166..37859012hg38UCSC Ensembl
Innerchr13:37851166..37859012hg38UCSC Ensembl
Outerchr13:37851149..37859068hg38UCSC Ensembl
chr13:38425303..38433149hg19UCSC Ensembl
Innerchr13:38425303..38433149hg19UCSC Ensembl
Outerchr13:38425286..38433205hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387847
hg197847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14697388, essv14697387
SamplesNA18853, HG01783
Known GenesTRPC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631810
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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