A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631516



Internal ID6671642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23220638..23346046hg38UCSC Ensembl
chr13:23794777..23920185hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38125409
hg19125409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14669427
SamplesHG03571
Known GenesSACS, SGCG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631516
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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