A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433145



Internal ID21090698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11739558..11969096hg38UCSC Ensembl
chr9:11739558..11969096hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38229539
hg19229539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7574n223
Supporting Variantsnssv18173901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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