A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596137



Internal ID21788180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119841184..119841268hg38UCSC Ensembl
chr8:120853424..120853508hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009534
Supporting Variants
Samples
Known GenesDSCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596137
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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