A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402006



Internal ID21059559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90845301..90851400hg38UCSC Ensembl
chr5:90141118..90147217hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214999
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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