A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14255547



Internal ID4257363
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627536
Supporting Variants
SamplesHG00324
Known GenesMMP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14255547
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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