A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287842



Internal ID20497060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196832770..196832875hg38UCSC Ensembl
chr2:197697494..197697599hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287842
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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