A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453448



Internal ID21111001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77492922..77499743hg38UCSC Ensembl
chr9:80107838..80114659hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg386822
hg196822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189833
Samples
Known GenesGNA14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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