A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841861



Internal ID22616796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170322697..170323696hg38UCSC Ensembl
chr5:169749701..169750700hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497664, nssv17497663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841861
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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