A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841344



Internal ID22616279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117449865..117452884hg38UCSC Ensembl
chr5:116785561..116788580hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg383020
hg193020
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493736
Samples
Known GenesLINC00992
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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