A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430853



Internal ID22488723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96324566..96324566hg38UCSC Ensembl
chr9:99086848..99086848hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951535
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430853
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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