A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386932



Internal ID22444802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32599517..32601273hg38UCSC Ensembl
chr1:33065118..33066874hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381757
hg191757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872074
Supporting Variants
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386932
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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