A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556056



Internal ID21880411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114241708..114241794hg38UCSC Ensembl
chr5:113577405..113577491hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556056
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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