A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435191



Internal ID21092744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22882401..23152700hg38UCSC Ensembl
chr9:22882400..23152699hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38270300
hg19270300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7648n223
Supporting Variantsnssv18229993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435191
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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