A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3537925



Internal ID22407117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159699777..159699777hg38UCSC Ensembl
chr6:160120809..160120809hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381671
hg191671
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14401228
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3537925
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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