A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601109



Internal ID21793156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104374578..104375346hg38UCSC Ensembl
chr12:104768356..104769124hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601109
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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