A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583935



Internal ID21775978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94393660..94394057hg38UCSC Ensembl
chr8:95405888..95406285hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010285
Supporting Variants
Samples
Known GenesRAD54B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583935
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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