A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632369



Internal ID7019178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62391235..62419208hg38UCSC Ensembl
chr13:62965368..62993341hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3827974
hg1927974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14768549
SamplesHG04180
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632369
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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