A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568537



Internal ID21760580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167859391..167860078hg38UCSC Ensembl
chr5:167286396..167287083hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009643
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568537
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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