A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367305



Internal ID22592974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15188988..15224212hg38UCSC Ensembl
chr1:15515484..15550708hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3835225
hg1935225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880428
Supporting Variants
Samples
Known GenesTMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367305
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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