A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511344



Internal ID22569296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125037974..125042098hg38UCSC Ensembl
chr9:127800253..127804377hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384125
hg194125
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866457
Supporting Variants
Samples
Known GenesSCAI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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