A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499004



Internal ID275985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6226222..6226307hg38UCSC Ensembl
chr11:6247452..6247537hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043241
Samples
Known GenesFAM160A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499004
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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