A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440616



Internal ID22498486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89052053..89055372hg38UCSC Ensembl
chr6:89761772..89765091hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383320
hg193320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440616
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004


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