A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614523



Internal ID21806570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12065280..12065411hg38UCSC Ensembl
chr12:12218214..12218345hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614523
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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