A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141507



Internal ID340704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75394779..75406779hg38UCSC Ensembl
chr7:75024053..75036063hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3812001
hg1912011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001088
Samples
Known GenesTRIM73, TRIM74
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141507
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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