A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10979332



Internal ID1347162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33778849..33787256hg38UCSC Ensembl
Innerchr3:33778874..33787231hg38UCSC Ensembl
Outerchr3:33778824..33787281hg38UCSC Ensembl
chr3:33820341..33828748hg19UCSC Ensembl
Innerchr3:33820366..33828723hg19UCSC Ensembl
Outerchr3:33820316..33828773hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg388408
hg198408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595796
Supporting Variants
SamplesHG01187
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10979332
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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