A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189762



Internal ID22340938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6331720..6332354hg38UCSC Ensembl
chr6:6331953..6332587hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463318
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)nsv3189762
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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