A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419619



Internal ID21077172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29068506..29078041hg38UCSC Ensembl
chr9:29068504..29078039hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg389536
hg199536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182391
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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