A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277665



Internal ID20486883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30869864..30870061hg38UCSC Ensembl
chr12:31022798..31022995hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277665
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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