A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625283



Internal ID7012118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7173169..7175257hg38UCSC Ensembl
Innerchr11:7173219..7175207hg38UCSC Ensembl
Outerchr11:7173114..7175312hg38UCSC Ensembl
chr11:7194400..7196488hg19UCSC Ensembl
Innerchr11:7194450..7196438hg19UCSC Ensembl
Outerchr11:7194345..7196543hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382089
hg192089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14013231, essv14013230, essv14013229, essv14013232, essv14013228, essv14013227
SamplesHG03086, HG02562, HG03556, HG02479, HG02887, HG03028
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625283
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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