A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514059



Internal ID22572017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66887162..66893303hg38UCSC Ensembl
chr9:40799538..40805679hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386142
hg196142
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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