A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088353



Internal ID21997586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97482634..97482634hg38UCSC Ensembl
chr12:97876412..97876412hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608533
Samples
Known GenesRMST
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088353
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