A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049607



Internal ID21958840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:237001925..237001925hg38UCSC Ensembl
chr1:237165225..237165225hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049607
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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