A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616069



Internal ID21564374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154755826..154755826hg38UCSC Ensembl
chr1:154728302..154728302hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061004
SamplesHG03732
Known GenesKCNN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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