A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085440



Internal ID21994673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91347963..91347963hg38UCSC Ensembl
chr9:94110245..94110245hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586718
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085440
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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