A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14013228



Internal ID2891180
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625283
Supporting Variants
SamplesHG02562
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14013228
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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