A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514173



Internal ID22572131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69857891..69862725hg38UCSC Ensembl
chr9:72472807..72477641hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg384835
hg194835
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862669
Supporting Variants
Samples
Known GenesC9orf135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514173
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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