A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11165526



Internal ID981972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142916678..142917536hg38UCSC Ensembl
Innerchr3:142916724..142917491hg38UCSC Ensembl
Outerchr3:142916633..142917582hg38UCSC Ensembl
chr3:142635520..142636378hg19UCSC Ensembl
Innerchr3:142635566..142636333hg19UCSC Ensembl
Outerchr3:142635475..142636424hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598012
Supporting Variants
SamplesHG00610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11165526
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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