A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574158



Internal ID21766201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132792243..132792243hg38UCSC Ensembl
chr6:133113382..133113382hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066554
Supporting Variants
Samples
Known GenesSLC18B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574158
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