A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828728



Internal ID22603663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171214382..171220256hg38UCSC Ensembl
chr1:171183521..171189395hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg385875
hg195875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828728
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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