A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908013



Internal ID6129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109843835..109861835hg38UCSC Ensembl
chr1:110386457..110404457hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908013
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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