A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858700



Internal ID22042343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2773783..2773783hg38UCSC Ensembl
chr6:2774017..2774017hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256581
Supporting Variants
Samples
Known GenesWRNIP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858700
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer