A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10980601



Internal ID3354685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35477533..35489324hg38UCSC Ensembl
Innerchr3:35477588..35489270hg38UCSC Ensembl
Outerchr3:35477479..35489379hg38UCSC Ensembl
chr3:35519025..35530816hg19UCSC Ensembl
Innerchr3:35519080..35530762hg19UCSC Ensembl
Outerchr3:35518971..35530871hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3811792
hg1911792
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595837
Supporting Variants
SamplesHG03007
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10980601
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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