A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568651



Internal ID21760694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132151281..132151346hg38UCSC Ensembl
chr7:131836040..131836105hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020080
Supporting Variants
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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