A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044566



Internal ID21953848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206782051..206782051hg38UCSC Ensembl
chr1:206955396..206955396hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044566
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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