A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841116



Internal ID22616051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130993478..130994477hg38UCSC Ensembl
chr5:130329171..130330170hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494887, nssv17494886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841116
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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