A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451923



Internal ID21109476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100807651..100810182hg38UCSC Ensembl
chr9:103569933..103572464hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382532
hg192532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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