A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260633



Internal ID20469851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18096893..18096947hg38UCSC Ensembl
chr12:18249827..18249881hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742507
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260633
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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