A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464492



Internal ID242369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13702311..13705254hg38UCSC Ensembl
chr6:13702543..13705486hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382944
hg192944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979031
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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