A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595654



Internal ID21544261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91633534..91641015hg38UCSC Ensembl
chr9:94395816..94403297hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387482
hg197482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163222
SamplesNA12329
Known GenesMIR3910-1, MIR3910-2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595654
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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