A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448590



Internal ID22506460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41280473..41280821hg38UCSC Ensembl
chr8:41137992..41138340hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919670
Supporting Variants
Samples
Known GenesSFRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448590
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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