A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272631



Internal ID20481849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13394341..13400418hg38UCSC Ensembl
chr12:13547275..13553352hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg386078
hg196078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272631
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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