A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614755



Internal ID21563060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150744433..150744433hg38UCSC Ensembl
chr1:150716909..150716909hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060778
SamplesHG00096
Known GenesCTSS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614755
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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