A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442372



Internal ID22500242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22835674..22837944hg38UCSC Ensembl
chr6:22835903..22838173hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382271
hg192271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442372
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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