A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443131



Internal ID21100684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130904662..130911859hg38UCSC Ensembl
chr9:133780049..133787246hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg387198
hg197198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222840
Samples
Known GenesFIBCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443131
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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