A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003935



Internal ID21913278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80145848..80145936hg38UCSC Ensembl
chr5:79441671..79441759hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541020
Samples
Known GenesSERINC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003935
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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