A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088229



Internal ID21997462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5868756..5868756hg38UCSC Ensembl
chr17:5772076..5772076hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631895
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088229
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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