A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830606



Internal ID22605541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63103560..63137696hg38UCSC Ensembl
chr1:63569231..63603367hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3834137
hg1934137
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830606
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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