A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876147



Internal ID22651107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32554663..32577058hg38UCSC Ensembl
chr1:33020264..33042659hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3822396
hg1922396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376985
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876147
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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