A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3536637



Internal ID22405863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13818937..13818937hg38UCSC Ensembl
chr2:13959062..13959062hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14420524
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)nsv3536637
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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