A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442324



Internal ID21099877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109161753..109164565hg38UCSC Ensembl
chr9:111924033..111926845hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173142
Samples
Known GenesFRRS1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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