A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892825



Internal ID169390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182805561..182805762hg38UCSC Ensembl
chr1:182774696..182774897hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451572
Supporting Variants
Samples
Known GenesNPL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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