A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359839



Internal ID22585508
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 Variantsnsv5967011
Supporting Variants
Samples
Known GenesUCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359839
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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