A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357255



Internal ID22582924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205647158..205648088hg38UCSC Ensembl
chr1:205616286..205617216hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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