A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286406



Internal ID20495624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8332953..8333012hg38UCSC Ensembl
chr10:8374916..8374975hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736517
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286406
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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