A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431565



Internal ID21089118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16920472..16965340hg38UCSC Ensembl
chr9:16920470..16965338hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3844869
hg1944869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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