A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828442



Internal ID22603377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185009061..185016134hg38UCSC Ensembl
chr1:184978193..184985266hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg387074
hg197074
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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