A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499350



Internal ID276324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3044689..3045500hg38UCSC Ensembl
chr11:3065919..3066730hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042136
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499350
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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