A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000938



Internal ID21910281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126844167..126844317hg38UCSC Ensembl
chr5:126179859..126180009hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000938
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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