A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841054



Internal ID22615989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123202737..123213441hg38UCSC Ensembl
chr5:122538431..122549135hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3810705
hg1910705
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841054
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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