A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10977917



Internal ID886307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32903650..32940604hg38UCSC Ensembl
Innerchr3:32903650..32940604hg38UCSC Ensembl
Outerchr3:32903377..32940862hg38UCSC Ensembl
chr3:32945142..32982096hg19UCSC Ensembl
Innerchr3:32945142..32982096hg19UCSC Ensembl
Outerchr3:32944869..32982354hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3836955
hg1936955
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595785
Supporting Variants
SamplesHG00476
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10977917
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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