A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631675



Internal ID6671800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30429199..30440721hg38UCSC Ensembl
chr13:31003336..31014858hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3811523
hg1911523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14680916, essv14680917
SamplesHG02389, HG02084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631675
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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