A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903971



Internal ID3466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66879963..66879967hg38UCSC Ensembl
chr1:67345646..67345650hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg385
hg195
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556394
Supporting Variants
Samples
Known GenesWDR78
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903971
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.008898


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