A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426321



Internal ID22484191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185592011..185592011hg38UCSC Ensembl
chr3:185309799..185309799hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965604
Supporting Variants
Samples
Known GenesSENP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426321
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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