A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012571



Internal ID21921914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180286145..180286723hg38UCSC Ensembl
chr5:179713145..179713723hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576513
Samples
Known GenesMAPK9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012571
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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