A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444691



Internal ID21102244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121681854..121686789hg38UCSC Ensembl
chr9:124444133..124449068hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384936
hg194936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236065
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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