A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555788



Internal ID21880143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78663849..78664795hg38UCSC Ensembl
chr5:77959672..77960618hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555788
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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