A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445712



Internal ID21103265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90410379..90412822hg38UCSC Ensembl
chr9:93172661..93175104hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382444
hg192444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445712
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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