A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529871



Internal ID21854228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236848018..236848018hg38UCSC Ensembl
chr2:237756661..237756661hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529871
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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