A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943647



Internal ID22719099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31774637..31789610hg38UCSC Ensembl
chr17:30101656..30116629hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3814974
hg1914974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943647
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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