A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597424



Internal ID6972270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112841722..112849363hg38UCSC Ensembl
Innerchr3:112841735..112849350hg38UCSC Ensembl
Outerchr3:112841709..112849376hg38UCSC Ensembl
chr3:112560569..112568210hg19UCSC Ensembl
Innerchr3:112560582..112568197hg19UCSC Ensembl
Outerchr3:112560556..112568223hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg387642
hg197642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11105139
SamplesHG03814
Known GenesCD200R1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597424
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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