A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523067



Internal ID21847426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239126499..239126499hg38UCSC Ensembl
chr1:239289799..239289799hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523067
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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