A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281555



Internal ID20490773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67731244..67731519hg38UCSC Ensembl
chr17:65727360..65727635hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748689
Supporting Variants
Samples
Known GenesNOL11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281555
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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