A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243484



Internal ID6028638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95374496..95376813hg38UCSC Ensembl
Innerchr11:95374546..95376763hg38UCSC Ensembl
Outerchr11:95374412..95376897hg38UCSC Ensembl
chr11:95107660..95109977hg19UCSC Ensembl
Innerchr11:95107710..95109927hg19UCSC Ensembl
Outerchr11:95107576..95110061hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382318
hg192318
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627347
Supporting Variants
SamplesNA19436
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243484
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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