A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900276



Internal ID975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28216196..28217426hg38UCSC Ensembl
chr1:28542707..28543937hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426504
Supporting Variants
Samples
Known GenesDNAJC8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900276
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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