A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510708



Internal ID22568659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110245751..110246850hg38UCSC Ensembl
chr9:113008031..113009130hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853600
Supporting Variants
Samples
Known GenesTXN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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