A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625082



Internal ID7011921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:805879..807017hg38UCSC Ensembl
Innerchr11:805879..807017hg38UCSC Ensembl
Outerchr11:805652..807289hg38UCSC Ensembl
chr11:805879..807017hg19UCSC Ensembl
Innerchr11:805879..807017hg19UCSC Ensembl
Outerchr11:805652..807289hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13992144
SamplesHG00536
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625082
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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