A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103095



Internal ID21484794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9716910..9716910hg38UCSC Ensembl
chr18:9716907..9716907hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662384
Supporting Variants
SamplesNA12329
Known GenesRAB31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103095
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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