A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455448



Internal ID21113001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36820871..36824874hg38UCSC Ensembl
chr9:36820868..36824871hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg384004
hg194004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186137
Samples
Known GenesMIR4475
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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