A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390376



Internal ID21047929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98163249..98381704hg38UCSC Ensembl
chr4:99084400..99302855hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38218456
hg19218456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121253
Samples
Known GenesRAP1GDS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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