A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702209



Internal ID125875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78765911..78766103hg38UCSC Ensembl
chr15:79058253..79058445hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147381
Supporting Variants
Samples
Known GenesADAMTS7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702209
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.088199


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