A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373756



Internal ID22316467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39466301..39469450hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212048
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)nssv14373756
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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