A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436904



Internal ID21094457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99996701..100001000hg38UCSC Ensembl
chr9:102758983..102763282hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226038
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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