A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455067



Internal ID21112620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69749510..69750235hg38UCSC Ensembl
chr9:72364426..72365151hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192064
Samples
Known GenesPTAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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