A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597846



Internal ID6984984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133576892..133578293hg38UCSC Ensembl
Innerchr3:133576951..133578234hg38UCSC Ensembl
Outerchr3:133576833..133578352hg38UCSC Ensembl
chr3:133295736..133297137hg19UCSC Ensembl
Innerchr3:133295795..133297078hg19UCSC Ensembl
Outerchr3:133295677..133297196hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11155289
SamplesNA19900
Known GenesCDV3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597846
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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