A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597873



Internal ID6985011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135644293..135648163hg38UCSC Ensembl
Innerchr3:135644343..135648113hg38UCSC Ensembl
Outerchr3:135644228..135648228hg38UCSC Ensembl
chr3:135363135..135367005hg19UCSC Ensembl
Innerchr3:135363185..135366955hg19UCSC Ensembl
Outerchr3:135363070..135367070hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383871
hg193871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11156671
SamplesHG00611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597873
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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