A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441393



Internal ID21098946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109983077..110215980hg38UCSC Ensembl
chr9:112745357..112978260hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38232904
hg19232904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227321
Samples
Known GenesAKAP2, C9orf152, PALM2-AKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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