A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007372



Internal ID21916715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112914299..112914468hg38UCSC Ensembl
chr5:112249996..112250165hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539205
Samples
Known GenesREEP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007372
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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