A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426298



Internal ID21083851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13441201..13442900hg38UCSC Ensembl
chr9:13441200..13442899hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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