A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008429



Internal ID21917772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113341292..113346405hg38UCSC Ensembl
chr5:112676989..112682102hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg385114
hg195114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543903
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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