A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541638



Internal ID21865993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17208456..17209758hg38UCSC Ensembl
chr5:17208565..17209867hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999021
Supporting Variants
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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