A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442278



Internal ID21099831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131225001..132519900hg38UCSC Ensembl
chr9:134100388..135395287hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381294900
hg191294900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236058
Samples
Known GenesC9orf171, FAM78A, MED27, NTNG2, NUP214, POMT1, PPAPDC3, PRRC2B, RAPGEF1, SETX, SNORD62A, SNORD62B, TTF1, UCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442278
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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