A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351889



Internal ID22577558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28216348..28218953hg38UCSC Ensembl
chr1:28542859..28545464hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880759
Supporting Variants
Samples
Known GenesDNAJC8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351889
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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