A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443912



Internal ID21101465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130500601..130517300hg38UCSC Ensembl
chr9:133375988..133392687hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3816700
hg1916700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226519
Samples
Known GenesASS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443912
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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