A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968161



Internal ID22743096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31859356..31859356hg38UCSC Ensembl
chr17:30186375..30186375hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968161
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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