A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541978



Internal ID21866333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95407254..95407382hg38UCSC Ensembl
chr5:94742958..94743086hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002776
Supporting Variants
Samples
Known GenesFAM81B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541978
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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