A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044288



Internal ID21953571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244518415..244518415hg38UCSC Ensembl
chr1:244681717..244681717hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527989
Samples
Known GenesC1orf101
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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