A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713343



Internal ID137009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45077054..45077164hg38UCSC Ensembl
chr17:43154422..43154532hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527116
Supporting Variants
Samples
Known GenesNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713343
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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