A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14255545



Internal ID4257361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102695893..102698786hg38UCSC Ensembl
Innerchr11:102695893..102698786hg38UCSC Ensembl
Outerchr11:102695816..102698909hg38UCSC Ensembl
chr11:102566624..102569517hg19UCSC Ensembl
Innerchr11:102566624..102569517hg19UCSC Ensembl
Outerchr11:102566547..102569640hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg382894
hg192894
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627535
Supporting Variants
SamplesHG00148
Known GenesMMP27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14255545
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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