A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452887



Internal ID21110440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133343917..133345115hg38UCSC Ensembl
chr9:136210772..136211970hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177107
Samples
Known GenesMED22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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