A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739598



Internal ID18713844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165826354..165826403hg38UCSC Ensembl
chr6:166239842..166239891hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739598
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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