A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13867089



Internal ID1774204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79414326..79464202hg38UCSC Ensembl
chr10:81174082..81223958hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3849877
hg1949877
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623910
Supporting Variants
SamplesHG01630
Known GenesZCCHC24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13867089
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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