A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714659



Internal ID138325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75785790..75785842hg38UCSC Ensembl
chr17:73781871..73781923hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145235
Supporting Variants
Samples
Known GenesUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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