A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3283626



Internal ID22381976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3090756..3091622hg38UCSC Ensembl
chr6:3090990..3091856hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14436244
SamplesHG00514
Known GenesRIPK1
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)nsv3283626
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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