A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616484



Internal ID21808531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104385721..104385721hg38UCSC Ensembl
chr12:104779499..104779499hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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