A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11070089



Internal ID4418853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95063569..95068105hg38UCSC Ensembl
Innerchr3:95063572..95068103hg38UCSC Ensembl
Outerchr3:95063567..95068108hg38UCSC Ensembl
chr3:94782413..94786949hg19UCSC Ensembl
Innerchr3:94782416..94786947hg19UCSC Ensembl
Outerchr3:94782411..94786952hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg384537
hg194537
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597039
Supporting Variants
SamplesHG03934
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11070089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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