A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098671



Internal ID22007904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50456460..50456460hg38UCSC Ensembl
chr17:48533821..48533821hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633336
Samples
Known GenesACSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098671
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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