A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010318



Internal ID21919661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90595114..90595167hg38UCSC Ensembl
chr5:89890931..89890984hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552697
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010318
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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