A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446105



Internal ID22503975
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 StatusS
Merged Variantsnsv5916727
Supporting Variants
Samples
Known GenesMIR3910-1, MIR3910-2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446105
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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