A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171390



Internal ID22331266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98013946..98014216hg38UCSC Ensembl
chr6:98461822..98462092hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456204
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)nsv3171390
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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