A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524440



Internal ID21848798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52928989..52928989hg38UCSC Ensembl
chr1:53394661..53394661hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048605
Supporting Variants
Samples
Known GenesSCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524440
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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