A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591370



Internal ID21783413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57133377..57133444hg38UCSC Ensembl
chr8:58045936..58046003hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591370
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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