A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056768



Internal ID21966002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54369748..54369748hg38UCSC Ensembl
chr1:54835421..54835421hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522492
Samples
Known GenesSSBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056768
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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