A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377614



Internal ID22435484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43975866..43975991hg38UCSC Ensembl
chr17:42053234..42053359hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937345
Supporting Variants
Samples
Known GenesPYY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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