A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071933



Internal ID21490223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97193181..97193248hg38UCSC Ensembl
chr10:98952938..98953005hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601323
Supporting Variants
SamplesNA19238
Known GenesARHGAP19-SLIT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071933
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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