A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388002



Internal ID22445872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39068336..39074170hg38UCSC Ensembl
chr1:39534008..39539842hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884476
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388002
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