A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843999



Internal ID22618934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121791104..121797550hg38UCSC Ensembl
chr6:122112250..122118696hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg386447
hg196447
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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