A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755335



Internal ID20531195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245269174..245269174hg38UCSC Ensembl
chr1:245432476..245432476hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275952
Samples
Known GenesKIF26B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755335
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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