A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846500



Internal ID22621435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97778458..97784633hg38UCSC Ensembl
chr6:98226334..98232509hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386176
hg196176
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846500
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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