A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448196



Internal ID21105749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132017030..132026814hg38UCSC Ensembl
chr9:134892417..134902201hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg389785
hg199785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177020
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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