A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000328



Internal ID21909671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51535796..51535868hg38UCSC Ensembl
chr5:50831630..50831702hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000328
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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