A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612679



Internal ID21804726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48014640..48014729hg38UCSC Ensembl
chr12:48408423..48408512hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612679
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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