A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595867



Internal ID6983185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36549578..36551822hg38UCSC Ensembl
Innerchr3:36549628..36551772hg38UCSC Ensembl
Outerchr3:36549480..36551920hg38UCSC Ensembl
chr3:36591070..36593314hg19UCSC Ensembl
Innerchr3:36591120..36593264hg19UCSC Ensembl
Outerchr3:36590972..36593412hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10980997
SamplesNA20803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595867
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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