A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925137



Internal ID21345207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243998721..243998721hg38UCSC Ensembl
chr1:244162023..244162023hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189449
SamplesHG002
Known GenesLOC339529
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925137
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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