A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14034136



Internal ID4035952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14540139..14591071hg38UCSC Ensembl
Innerchr11:14540139..14591071hg38UCSC Ensembl
Outerchr11:14539639..14591571hg38UCSC Ensembl
chr11:14561685..14612617hg19UCSC Ensembl
Innerchr11:14561685..14612617hg19UCSC Ensembl
Outerchr11:14561185..14613117hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3850933
hg1950933
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625424
Supporting Variants
SamplesHG02221
Known GenesPSMA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14034136
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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