A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282406



Internal ID20491624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97160087..97163543hg38UCSC Ensembl
chr7:96789399..96792855hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383457
hg193457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741848
Supporting Variants
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282406
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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