A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632578



Internal ID7019388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67957852..68008706hg38UCSC Ensembl
chr13:68531984..68582838hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3850855
hg1950855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14782621
SamplesHG02947
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632578
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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