A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11055710



Internal ID4076379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82806631..82812017hg38UCSC Ensembl
Innerchr3:82806649..82812000hg38UCSC Ensembl
Outerchr3:82806614..82812035hg38UCSC Ensembl
chr3:82855782..82861168hg19UCSC Ensembl
Innerchr3:82855800..82861151hg19UCSC Ensembl
Outerchr3:82855765..82861186hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg385387
hg195387
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596773
Supporting Variants
SamplesHG03708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11055710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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