A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562940



Internal ID21887295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143861822..143861822hg38UCSC Ensembl
chr6:144182959..144182959hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063238
Supporting Variants
Samples
Known GenesLTV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562940
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