A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14178524



Internal ID6156775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61991825..61992422hg38UCSC Ensembl
Innerchr11:61991848..61992400hg38UCSC Ensembl
Outerchr11:61991803..61992445hg38UCSC Ensembl
chr11:61759297..61759894hg19UCSC Ensembl
Innerchr11:61759320..61759872hg19UCSC Ensembl
Outerchr11:61759275..61759917hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626588
Supporting Variants
SamplesNA19700
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14178524
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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