A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438874



Internal ID21096427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67604901..67613700hg38UCSC Ensembl
chr9:44751597..46272229hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388800
hg191520633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227593
Samples
Known GenesFAM27A, FAM27C, FAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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