A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239755



Internal ID22044365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132255190..132255190hg38UCSC Ensembl
chr7:131939949..131939949hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839126
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239755
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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