A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436168



Internal ID21093721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63288401..63331500hg38UCSC Ensembl
chr9:67243373..67286472hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3843100
hg1943100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220879
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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