A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180177



Internal ID22335942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6372671..6372726hg38UCSC Ensembl
chr8:6230192..6230247hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14391575
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)nsv3180177
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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