A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627350



Internal ID7014180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95442258..95448343hg38UCSC Ensembl
Innerchr11:95442258..95448343hg38UCSC Ensembl
Outerchr11:95441758..95448843hg38UCSC Ensembl
chr11:95175422..95181507hg19UCSC Ensembl
Innerchr11:95175422..95181507hg19UCSC Ensembl
Outerchr11:95174922..95182007hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14243538, essv14243545, essv14243542, essv14243543, essv14243540, essv14243546, essv14243544, essv14243536, essv14243537, essv14243539, essv14243541
SamplesHG03558, NA20359, HG02471, HG03055, HG02322, HG03382, NA19436, HG02759, NA19019, NA20362, HG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627350
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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