A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157344



Internal ID21472907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108131543..108131543hg38UCSC Ensembl
chr9:110893823..110893823hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633730
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157344
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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