A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063686



Internal ID21441490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245269213..245269213hg38UCSC Ensembl
chr1:245432515..245432515hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609735
Supporting Variants
SamplesHG00732
Known GenesKIF26B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063686
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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