A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633088



Internal ID7019898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89082044..89180501hg38UCSC Ensembl
chr13:89734298..89832755hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3898458
hg1998458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14837104
SamplesNA18566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633088
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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