A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997338



Internal ID65767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44211125..44212246hg38UCSC Ensembl
chr7:44250724..44251845hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483016
Supporting Variants
Samples
Known GenesYKT6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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