A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514943



Internal ID22572902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97076767..97082556hg38UCSC Ensembl
chr9:99839049..99844838hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385790
hg195790
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856932
Supporting Variants
Samples
Known GenesLOC340508
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514943
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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