A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640753



Internal ID21589058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97079760..97079760hg38UCSC Ensembl
chr9:99842042..99842042hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163193
SamplesHG00512
Known GenesLOC340508
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640753
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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