A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034934



Internal ID91014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44113999..44153023hg38UCSC Ensembl
chr10:44609447..44648471hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3839025
hg1939025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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