A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352309



Internal ID22577978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205606416..205607463hg38UCSC Ensembl
chr1:205575544..205576591hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352309
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