A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997245



Internal ID21906588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37659820..37660141hg38UCSC Ensembl
chr4:37661442..37661763hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547900
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997245
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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