A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664160



Internal ID3665976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118426..174375hg38UCSC Ensembl
chr10:164366..220315hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3855950
hg1955950
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622070
Supporting Variants
SamplesNA20872
Known GenesZMYND11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664160
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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