A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000397



Internal ID21909740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8004880..8004934hg38UCSC Ensembl
chr5:8004993..8005047hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000397
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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