A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10901982



Internal ID4407664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3063880..3065154hg38UCSC Ensembl
Innerchr3:3063892..3065142hg38UCSC Ensembl
Outerchr3:3063868..3065166hg38UCSC Ensembl
chr3:3105564..3106838hg19UCSC Ensembl
Innerchr3:3105576..3106826hg19UCSC Ensembl
Outerchr3:3105552..3106850hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595050
Supporting Variants
SamplesHG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10901982
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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