A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436927



Internal ID21094480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92518037..92519281hg38UCSC Ensembl
chr9:95280319..95281563hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184006
Samples
Known GenesCENPP, ECM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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