A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631699



Internal ID7018507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31578032..31652880hg38UCSC Ensembl
chr13:32152169..32227017hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3874849
hg1974849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14683340, essv14683341
SamplesHG01396, HG01089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631699
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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