A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839127



Internal ID22022770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132416008..132416008hg38UCSC Ensembl
chr7:132100767..132100767hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239756
Supporting Variants
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839127
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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