A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398603



Internal ID21056156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90957716..90958816hg38UCSC Ensembl
chr5:90253533..90254633hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133762
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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