A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085633



Internal ID21994866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83220250..83220250hg38UCSC Ensembl
chr9:85835165..85835165hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085633
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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