A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192908



Internal ID22343428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1291594..1291724hg38UCSC Ensembl
chr6:1291829..1291959hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7707n152
Supporting Variantsnssv14461628
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192908
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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