A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057338



Internal ID21966571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153770059..153770059hg38UCSC Ensembl
chr1:153742535..153742535hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534350
Samples
Known GenesINTS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057338
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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