A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846501



Internal ID22621436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97779108..97782288hg38UCSC Ensembl
chr6:98226984..98230164hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383181
hg193181
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846501
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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