A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460048



Internal ID238046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52739932..52742045hg38UCSC Ensembl
chr6:52604730..52606843hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg382114
hg192114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985897
Samples
Known GenesGSTA7P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460048
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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