A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846111



Internal ID22621046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84672216..84678126hg38UCSC Ensembl
chr6:85381934..85387844hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg385911
hg195911
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508437, nssv17508438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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