A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472806



Internal ID250508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89084289..89084366hg38UCSC Ensembl
chr6:89794008..89794085hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735591
Samples
Known GenesPNRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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