A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871491



Internal ID22646429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159150320..159155845hg38UCSC Ensembl
chr1:159120110..159125635hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg385526
hg195526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871491
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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