A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828051



Internal ID22602986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158233507..158235894hg38UCSC Ensembl
chr1:158203297..158205684hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382388
hg192388
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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