A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906773



Internal ID5300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98726219..98737307hg38UCSC Ensembl
chr1:99191775..99202863hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3811089
hg1911089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419457
Supporting Variants
Samples
Known GenesSNX7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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