A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993488



Internal ID63111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15708864..15862967hg38UCSC Ensembl
chr7:15748489..15902592hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38154104
hg19154104
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993488
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