A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13716163



Internal ID4027381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23478938..23499029hg38UCSC Ensembl
chr10:23767867..23787958hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3820092
hg1920092
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622612
Supporting Variants
SamplesHG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13716163
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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