A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766189



Internal ID18393749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25529650..25529783hg38UCSC Ensembl
Outerchr6:25529642..25529791hg38UCSC Ensembl
Innerchr6:25529878..25530011hg19UCSC Ensembl
Outerchr6:25529870..25530019hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567442
Supporting Variants
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766189
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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