A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287601



Internal ID20496819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95074405..95074547hg38UCSC Ensembl
chr8:96086633..96086775hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287601
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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