A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442281



Internal ID22500151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39232714..39237589hg38UCSC Ensembl
chr6:39200490..39205365hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384876
hg194876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442281
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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