A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605572



Internal ID21797619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108436096..108437431hg38UCSC Ensembl
chr12:108829873..108831208hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605572
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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