A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14009009



Internal ID4482460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6145181..6157957hg38UCSC Ensembl
Innerchr11:6145181..6157957hg38UCSC Ensembl
Outerchr11:6144681..6158457hg38UCSC Ensembl
chr11:6166411..6179187hg19UCSC Ensembl
Innerchr11:6166411..6179187hg19UCSC Ensembl
Outerchr11:6165911..6179687hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812777
hg1912777
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625261
Supporting Variants
SamplesHG03985
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14009009
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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