A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327423



Internal ID22267020
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207368
Supporting Variants
SamplesNA19238
Known GenesELOVL2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327423
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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