A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595083



Internal ID21787126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42644069..42644382hg38UCSC Ensembl
chr8:42499212..42499525hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595083
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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