A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631363



Internal ID6671490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18806777..18849024hg38UCSC Ensembl
chr13:19380917..19423164hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3842248
hg1942248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14655140
SamplesHG01530
Known GenesANKRD20A9P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631363
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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