A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902087



Internal ID22677241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88654585..88654676hg38UCSC Ensembl
chr6:89364304..89364395hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437022
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902087
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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