A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563942



Internal ID21888297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37730409..37731339hg38UCSC Ensembl
chr8:37587927..37588857hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563942
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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