A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913337



Internal ID22688553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127864217..127871420hg38UCSC Ensembl
chr9:130626496..130633699hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387204
hg197204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435451
Samples
Known GenesAK1, MIR4672
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913337
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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