A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089272



Internal ID21998505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13782438..13782438hg38UCSC Ensembl
chr17:13685755..13685755hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089272
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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