A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945020



Internal ID21365089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187718048..187718048hg38UCSC Ensembl
chr3:187435836..187435836hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191011
SamplesHG002
Known GenesLOC100131635
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945020
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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