A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766373



Internal ID18740619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35425235..35425354hg38UCSC Ensembl
Outerchr6:35425222..35425363hg38UCSC Ensembl
Innerchr6:35393012..35393131hg19UCSC Ensembl
Outerchr6:35392999..35393140hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567626
Supporting Variants
Samples
Known GenesPPARD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766373
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer