A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463079



Internal ID22215594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68257829..68257889hg38UCSC Ensembl
chr15:68550167..68550227hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222590
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14463079
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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