A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607196



Internal ID21799243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85395374..85395374hg38UCSC Ensembl
chr13:85969509..85969509hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081567
Supporting Variants
Samples
Known GenesLINC00351
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607196
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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