A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447491



Internal ID21105044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106403501..106405100hg38UCSC Ensembl
chr9:109165782..109167381hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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