A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484471



Internal ID261882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45166835..45166969hg38UCSC Ensembl
chr7:45206434..45206568hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997356
Samples
Known GenesRAMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484471
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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