A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437874



Internal ID21095427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135865734..135958903hg38UCSC Ensembl
chr9:138757580..138850749hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3893170
hg1993170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235838
Samples
Known GenesCAMSAP1, UBAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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