A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626169



Internal ID6666318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44738872..44740606hg38UCSC Ensembl
Innerchr11:44738875..44740604hg38UCSC Ensembl
Outerchr11:44738870..44740609hg38UCSC Ensembl
chr11:44760422..44762156hg19UCSC Ensembl
Innerchr11:44760425..44762154hg19UCSC Ensembl
Outerchr11:44760420..44762159hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14116495
SamplesHG00759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626169
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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