A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549446



Internal ID21873801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79469765..79471604hg38UCSC Ensembl
chr5:78765588..78767427hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002775
Supporting Variants
Samples
Known GenesHOMER1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549446
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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