A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633388



Internal ID6673510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103031638..103052594hg38UCSC Ensembl
chr13:103683988..103704944hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3820957
hg1920957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv363e214
Supporting Variantsessv14881022, essv14881023
SamplesHG01710, NA19779
Known GenesSLC10A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633388
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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