A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845058



Internal ID22619993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170052336..170057843hg38UCSC Ensembl
chr6:170367560..170373067hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385508
hg195508
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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