A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207368



Internal ID22355765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11059342..11059960hg38UCSC Ensembl
chr6:11059575..11060193hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327423, nssv14327422
SamplesNA19238, HG00731
Known GenesELOVL2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207368
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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