A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631806



Internal ID7018615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37814713..37830280hg38UCSC Ensembl
Innerchr13:37814732..37830261hg38UCSC Ensembl
Outerchr13:37814694..37830299hg38UCSC Ensembl
chr13:38388850..38404417hg19UCSC Ensembl
Innerchr13:38388869..38404398hg19UCSC Ensembl
Outerchr13:38388831..38404436hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3815568
hg1915568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14697359
SamplesNA19835
Known GenesTRPC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631806
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