A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061061



Internal ID21478313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165835314..165835314hg38UCSC Ensembl
chr1:165804551..165804551hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624134
Supporting Variants
SamplesHG03486
Known GenesUCK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061061
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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