A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565816



Internal ID21757781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33513955..33515013hg38UCSC Ensembl
chr8:33371473..33372531hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565816
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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