A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944624



Internal ID21364694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222090176..222090176hg38UCSC Ensembl
chr1:222263518..222263518hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190966
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944624
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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