A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944189



Internal ID21364258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161095805..161095805hg38UCSC Ensembl
chr2:161952316..161952316hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187617
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944189
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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