A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095449



Internal ID22004682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19557554..19557554hg38UCSC Ensembl
chr17:19460867..19460867hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382762
hg192762
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621164
Samples
Known GenesSLC47A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095449
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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