A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511693



Internal ID22569645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133391606..133394847hg38UCSC Ensembl
chr9:136257382..136259974hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383242
hg192593
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860288
Supporting Variants
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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