A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830066



Internal ID22605001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47161346..47167104hg38UCSC Ensembl
chr1:47627018..47632776hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg385759
hg195759
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466539, nssv17465740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830066
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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