A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002657



Internal ID69387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132637606..132655247hg38UCSC Ensembl
chr7:132322365..132340006hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3817642
hg1917642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482195
Supporting Variants
Samples
Known GenesFLJ40288, PLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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