A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631523



Internal ID6671649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23479493..23611329hg38UCSC Ensembl
chr13:24053632..24185468hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38131837
hg19131837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14669655
SamplesHG03571
Known GenesLINC00327, TNFRSF19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631523
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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