A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437552



Internal ID21095105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110159107..110309502hg38UCSC Ensembl
chr9:112921387..113071782hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38150396
hg19150396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7908n223
Supporting Variantsnssv18236310
Samples
Known GenesAKAP2, C9orf152, PALM2-AKAP2, TXN, TXNDC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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