A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953165



Internal ID21373234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211609099..211609099hg38UCSC Ensembl
chr1:211782441..211782441hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189691
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953165
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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