A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625936



Internal ID7012770
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090420, essv14090428, essv14090426, essv14090427, essv14090417, essv14090425, essv14090423, essv14090418, essv14090422, essv14090419, essv14090424, essv14090421
SamplesNA20514, HG02648, HG02691, HG04001, HG02786, NA20757, HG03945, HG03969, HG01685, HG04099, HG03894, HG03985
Known GenesTRIM44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625936
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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