A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161025



Internal ID21462864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14850336..14850434hg38UCSC Ensembl
chr9:14850334..14850432hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593835
Supporting Variants
SamplesHG03009
Known GenesFREM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161025
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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