A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14182142



Internal ID3679324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63068931..63076767hg38UCSC Ensembl
Innerchr11:63068948..63076750hg38UCSC Ensembl
Outerchr11:63068914..63076784hg38UCSC Ensembl
chr11:62836403..62844239hg19UCSC Ensembl
Innerchr11:62836420..62844222hg19UCSC Ensembl
Outerchr11:62836386..62844256hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg387837
hg197837
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626622
Supporting Variants
SamplesHG03280
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14182142
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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