A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002487



Internal ID21911830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109450871..109456547hg38UCSC Ensembl
chr5:108786572..108792248hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg385677
hg195677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002487
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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