A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430607



Internal ID21088160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27820054..27821920hg38UCSC Ensembl
chr9:27820052..27821918hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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