A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627536



Internal ID6667683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102837235..102838743hg38UCSC Ensembl
Innerchr11:102837235..102838743hg38UCSC Ensembl
Outerchr11:102836923..102839053hg38UCSC Ensembl
chr11:102707966..102709474hg19UCSC Ensembl
Innerchr11:102707966..102709474hg19UCSC Ensembl
Outerchr11:102707654..102709784hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14255548, essv14255547, essv14255546, essv14255549
SamplesHG00330, HG02490, HG00324, HG00288
Known GenesMMP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627536
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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