A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950635



Internal ID21370705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106272428..106272428hg38UCSC Ensembl
chr12:106666206..106666206hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193324
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950635
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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