A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095556



Internal ID22004789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40315127..40315127hg38UCSC Ensembl
chr17:38471379..38471379hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621432
Samples
Known GenesRARA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095556
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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