A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002776



Internal ID21912119
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 StatusM
Merged Variants
Supporting Variantsnssv17541978
Samples
Known GenesFAM81B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002776
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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