A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581154



Internal ID21773197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64448472..64448813hg38UCSC Ensembl
chr8:65361029..65361370hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581154
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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