A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142633



Internal ID341834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133203440..133203518hg38UCSC Ensembl
chr7:132888198..132888276hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142633
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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