A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444205



Internal ID21101758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128653790..128655338hg38UCSC Ensembl
chr9:131416069..131417617hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219235
Samples
Known GenesWDR34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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