A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000072



Internal ID21909415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6570992..6571069hg38UCSC Ensembl
chr5:6571105..6571182hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000072
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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