A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10959866



Internal ID816221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26462312..26466078hg38UCSC Ensembl
Innerchr3:26462312..26466078hg38UCSC Ensembl
Outerchr3:26462046..26466295hg38UCSC Ensembl
chr3:26503803..26507569hg19UCSC Ensembl
Innerchr3:26503803..26507569hg19UCSC Ensembl
Outerchr3:26503537..26507786hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg383767
hg193767
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595641
Supporting Variants
SamplesHG00404
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10959866
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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