A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631808



Internal ID7018617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37837215..37838627hg38UCSC Ensembl
Innerchr13:37837225..37838618hg38UCSC Ensembl
Outerchr13:37837206..37838637hg38UCSC Ensembl
chr13:38411352..38412764hg19UCSC Ensembl
Innerchr13:38411362..38412755hg19UCSC Ensembl
Outerchr13:38411343..38412774hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381413
hg191413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14697385
SamplesNA19658
Known GenesTRPC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631808
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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