A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906774



Internal ID5301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98733934..98734096hg38UCSC Ensembl
chr1:99199490..99199652hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430115
Supporting Variants
Samples
Known GenesSNX7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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