A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510596



Internal ID22568547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105713634..105716633hg38UCSC Ensembl
chr9:108475915..108478914hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861193
Supporting Variants
Samples
Known GenesTMEM38B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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