A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392659



Internal ID22450529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202050935..202050935hg38UCSC Ensembl
chr2:202915658..202915658hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954637
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392659
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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