A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633578



Internal ID7020387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112330772..112441098hg38UCSC Ensembl
chr13:112985086..113095412hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38110327
hg19110327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14900016
SamplesHG03439
Known GenesSPACA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633578
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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