A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3290100



Internal ID22387692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2939009..2939080hg38UCSC Ensembl
chr19:2939007..2939078hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14407343
SamplesNA19240
Known GenesZNF77
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)nsv3290100
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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