A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598634



Internal ID6985770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170711714..170713499hg38UCSC Ensembl
Innerchr3:170711764..170713449hg38UCSC Ensembl
Outerchr3:170711658..170713555hg38UCSC Ensembl
chr3:170429503..170431288hg19UCSC Ensembl
Innerchr3:170429553..170431238hg19UCSC Ensembl
Outerchr3:170429447..170431344hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11224321
SamplesHG02284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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