A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906192



Internal ID22681389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113386148..113386354hg38UCSC Ensembl
chr6:113707350..113707556hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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