A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570605



Internal ID21762648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176961990..176962123hg38UCSC Ensembl
chr5:176388991..176389124hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011835
Supporting Variants
Samples
Known GenesUIMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570605
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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