A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3281910



Internal ID22380239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151599283..151599550hg38UCSC Ensembl
chr1:151571759..151572026hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv417n152
Supporting Variantsnssv14432033
SamplesHG00514
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)nsv3281910
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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