A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376625



Internal ID22602294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32485447..32485447hg38UCSC Ensembl
chr1:32951048..32951048hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951580
Supporting Variants
Samples
Known GenesZBTB8B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376625
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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