A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950461



Internal ID21370530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:197206..197206hg38UCSC Ensembl
chr12:306372..306372hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191804, nssv15193907
SamplesHG002
Known GenesSLC6A12
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950461
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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