A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626168



Internal ID7013002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44720926..44725736hg38UCSC Ensembl
Innerchr11:44720938..44725724hg38UCSC Ensembl
Outerchr11:44720914..44725748hg38UCSC Ensembl
chr11:44742476..44747286hg19UCSC Ensembl
Innerchr11:44742488..44747274hg19UCSC Ensembl
Outerchr11:44742464..44747298hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg384811
hg194811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14116494, essv14116491, essv14116492, essv14116493
SamplesNA19457, NA20287, HG02887, HG03446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626168
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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