A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13761343



Internal ID6656607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42293750..42452381hg38UCSC Ensembl
chr10:42789198..42947829hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38158632
hg19158632
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623002
Supporting Variants
SamplesNA20804
Known GenesCCNYL2, LOC441666
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13761343
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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