A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517880



Internal ID21842239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235155862..235155862hg38UCSC Ensembl
chr1:235319177..235319177hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042025
Supporting Variants
Samples
Known GenesRBM34
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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