A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715621



Internal ID139287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81893133..81901133hg38UCSC Ensembl
chr17:79851009..79859009hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144462
Supporting Variants
Samples
Known GenesANAPC11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715621
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.020538


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