A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419021



Internal ID22476891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114164699..114517903hg38UCSC Ensembl
chr6:114485863..114839067hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38353205
hg19353205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419021
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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