A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10902160



Internal ID1012462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3370233..3376897hg38UCSC Ensembl
Innerchr3:3370262..3376869hg38UCSC Ensembl
Outerchr3:3370205..3376926hg38UCSC Ensembl
chr3:3411917..3418581hg19UCSC Ensembl
Innerchr3:3411946..3418553hg19UCSC Ensembl
Outerchr3:3411889..3418610hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg386665
hg196665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595059
Supporting Variants
SamplesHG00632
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10902160
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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