A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604271



Internal ID21796318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91244607..91244607hg38UCSC Ensembl
chr13:91896861..91896861hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604271
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer