A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593723



Internal ID21785766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61409363..61409363hg38UCSC Ensembl
chr9:40552978..40552978hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095639
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593723
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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