A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611202



Internal ID21803249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98510204..98510852hg38UCSC Ensembl
chr12:98903982..98904630hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611202
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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