A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376105



Internal ID22319851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137703656..137703793hg38UCSC Ensembl
chr6:138024793..138024930hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191369
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376105
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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