A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010609



Internal ID74701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37770705..37770824hg38UCSC Ensembl
chr8:37628223..37628342hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487173
Supporting Variants
Samples
Known GenesPROSC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010609
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00921


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