A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13765144



Internal ID3766960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44993759..45028111hg38UCSC Ensembl
chr10:45489207..45523559hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3834353
hg1934353
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623080
Supporting Variants
SamplesHG00640
Known GenesC10orf25, RASSF4, ZNF22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13765144
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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