A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567441



Internal ID18421831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25429755..25429885hg38UCSC Ensembl
Outerchr6:25429739..25429886hg38UCSC Ensembl
Innerchr6:25429983..25430113hg19UCSC Ensembl
Outerchr6:25429967..25430114hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766188
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567441
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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