A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428452



Internal ID22486322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21437701..21437701hg38UCSC Ensembl
chr3:21479193..21479193hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955976
Supporting Variants
Samples
Known GenesZNF385D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428452
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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