A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433191



Internal ID21090744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4684807..4740061hg38UCSC Ensembl
chr9:4684807..4740061hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3855255
hg1955255
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234265
Samples
Known GenesAK3, CDC37L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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