A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551479



Internal ID21875834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65490163..65492381hg38UCSC Ensembl
chr5:64785990..64788208hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382219
hg192219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551479
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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