A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616768



Internal ID21808815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93404509..93404720hg38UCSC Ensembl
chr12:93798285..93798496hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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