A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842329



Internal ID22617264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25926019..25929806hg38UCSC Ensembl
chr5:25926128..25929915hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg383788
hg193788
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842329
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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