A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567319



Internal ID18421709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16265584..16265681hg38UCSC Ensembl
chr6:16265815..16265912hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766066
Samples
Known GenesGMPR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567319
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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