A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908123



Internal ID6206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8387309..8415484hg38UCSC Ensembl
chr1:8447369..8475544hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3828176
hg1928176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432845
Supporting Variants
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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