A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449250



Internal ID21106803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83990317..83990858hg38UCSC Ensembl
chr9:86605232..86605773hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194163
Samples
Known GenesRMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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