A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949110



Internal ID21369179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84756772..84756772hg38UCSC Ensembl
chr1:85222455..85222455hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195517
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949110
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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