A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041199



Internal ID95167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127754278..127793709hg38UCSC Ensembl
chr10:129552542..129591973hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3839432
hg1939432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041199
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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