A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627893



Internal ID7014718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119634114..119639011hg38UCSC Ensembl
Innerchr11:119634114..119639011hg38UCSC Ensembl
Outerchr11:119633898..119639344hg38UCSC Ensembl
chr11:119504825..119509721hg19UCSC Ensembl
Innerchr11:119504825..119509721hg19UCSC Ensembl
Outerchr11:119504609..119510054hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384898
hg194897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14293361, essv14293364, essv14293360, essv14293362, essv14293363
SamplesHG00306, HG04162, HG04200, HG03727, NA20849
Known GenesPVRL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627893
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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