A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447922



Internal ID21105475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75594301..75595900hg38UCSC Ensembl
chr9:78209217..78210816hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188357
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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