A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094498



Internal ID22003731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97900510..97900510hg38UCSC Ensembl
chr10:99660267..99660267hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592230
Samples
Known GenesCRTAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094498
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