A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13765099



Internal ID3766915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44835801..44865096hg38UCSC Ensembl
chr10:45331249..45360544hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3829296
hg1929296
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623072
Supporting Variants
SamplesNA20513
Known GenesTMEM72-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13765099
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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