A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103059



Internal ID22012292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33215608..33215608hg38UCSC Ensembl
chr19:33706514..33706514hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624211
Samples
Known GenesSLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103059
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