A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044457



Internal ID21953739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87362017..87362017hg38UCSC Ensembl
chr1:87827700..87827700hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537494
Samples
Known GenesLOC100505768
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044457
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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