A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454151



Internal ID22248782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821830..150821926hg38UCSC Ensembl
chr3:150539617..150539713hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3281841
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454151
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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