A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611013



Internal ID21559318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170956719..170956719hg38UCSC Ensembl
chr1:170925860..170925860hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg382839
hg192839
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061325
SamplesHG02011
Known GenesMROH9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611013
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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