A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871489



Internal ID22646427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59131751..59132016hg38UCSC Ensembl
chr1:59597423..59597688hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369711
Samples
Known GenesHSD52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871489
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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