A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413872



Internal ID21071425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90555322..90564205hg38UCSC Ensembl
chr5:89851139..89860022hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg388884
hg198884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134930
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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