A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532138



Internal ID21856494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160034378..160034378hg38UCSC Ensembl
chr1:160004168..160004168hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg384033
hg194033
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532138
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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