A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902436



Internal ID22677595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52638462..52878278hg38UCSC Ensembl
chr6:52503260..52743076hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38239817
hg19239817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435835
Samples
Known GenesGSTA1, GSTA2, GSTA5, GSTA7P, LOC730101, TMEM14A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902436
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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