A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626171



Internal ID6666320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45140524..45143543hg38UCSC Ensembl
Innerchr11:45140545..45143523hg38UCSC Ensembl
Outerchr11:45140504..45143564hg38UCSC Ensembl
chr11:45162075..45165094hg19UCSC Ensembl
Innerchr11:45162096..45165074hg19UCSC Ensembl
Outerchr11:45162055..45165115hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383020
hg193020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14116497, essv14116498
SamplesHG02613, HG00306
Known GenesPRDM11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626171
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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