A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567485



Internal ID21759528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159050140..159050203hg38UCSC Ensembl
chr5:158477148..158477211hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017037
Supporting Variants
Samples
Known GenesEBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567485
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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