A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464388



Internal ID242266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88713726..88717665hg38UCSC Ensembl
chr6:89423445..89427384hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383940
hg193940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986835
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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