A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866689



Internal ID22641624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129629963..129632062hg38UCSC Ensembl
chr9:132392242..132394341hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511482
Samples
Known GenesNTMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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