A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563670



Internal ID21888025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130673805..130673904hg38UCSC Ensembl
chr7:130358645..130358744hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016806
Supporting Variants
Samples
Known GenesTSGA13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563670
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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