A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627535



Internal ID6667682
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14255545
SamplesHG00148
Known GenesMMP27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627535
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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