A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946056



Internal ID21366125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25529499..25529499hg38UCSC Ensembl
chr1:25855990..25855990hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192738
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946056
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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