A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954169



Internal ID21374240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65741580..65741580hg38UCSC Ensembl
chr12:66135360..66135360hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191968
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954169
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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