A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034967



Internal ID91038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44512441..44512507hg38UCSC Ensembl
chr10:45007889..45007955hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034967
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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