A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11105043



Internal ID1106859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112807512..112904954hg38UCSC Ensembl
chr3:112526359..112623801hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3897443
hg1997443
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597421
Supporting Variants
SamplesHG04202
Known GenesCD200R1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11105043
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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