A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448886



Internal ID21106439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40905230..40929456hg38UCSC Ensembl
chr9:66858258..69002685hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3824227
hg192144428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7716n223
Supporting Variantsnssv18227719
Samples
Known GenesANKRD20A1, ANKRD20A3, AQP7P1, FAM27B, FAM27E3, LOC100132352, LOC286297, LOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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