A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284497



Internal ID20493715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73037241..73037305hg38UCSC Ensembl
chr8:73949476..73949540hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747601
Supporting Variants
Samples
Known GenesTERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284497
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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