A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032578



Internal ID89404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18549716..18653624hg38UCSC Ensembl
chr10:18838645..18942553hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38103909
hg19103909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475053
Supporting Variants
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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