A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090417



Internal ID1814273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35691694..35696547hg38UCSC Ensembl
Innerchr11:35692194..35696047hg38UCSC Ensembl
Outerchr11:35690694..35697547hg38UCSC Ensembl
chr11:35713242..35718095hg19UCSC Ensembl
Innerchr11:35713742..35717595hg19UCSC Ensembl
Outerchr11:35712242..35719095hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384854
hg194854
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625936
Supporting Variants
SamplesHG01685
Known GenesTRIM44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090417
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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