A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033001



Internal ID89702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33211289..33211375hg38UCSC Ensembl
chr10:33500217..33500303hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491871
Supporting Variants
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033001
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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