A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086726



Internal ID21995959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15175975..15175975hg38UCSC Ensembl
chr17:15079292..15079292hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086726
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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