A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914885



Internal ID10678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61132959..61132983hg38UCSC Ensembl
chr2:61360094..61360118hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3825
hg1925
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558023
Supporting Variants
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914885
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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