A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7716n223



Internal ID22810684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40905230..40930876hg38UCSC Ensembl
chr9:66858258..69004105hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3825647
hg192145848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6438907, nsv6448886
Samples
Known GenesANKRD20A1, ANKRD20A3, AQP7P1, FAM27B, FAM27E3, LOC100132352, LOC286297, LOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7716n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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