A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422206



Internal ID21079759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16020626..16068892hg38UCSC Ensembl
chr9:16020624..16068890hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3848267
hg1948267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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