A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445101



Internal ID22502971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33513955..33515012hg38UCSC Ensembl
chr8:33371473..33372530hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445101
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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