A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505672



Internal ID22563616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11866804..11867940hg38UCSC Ensembl
chr8:11724313..11725449hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863850
Supporting Variants
Samples
Known GenesCTSB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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