A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938885



Internal ID21358954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29253250..29253250hg38UCSC Ensembl
chr12:29406183..29406183hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191890
SamplesHG002
Known GenesFAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938885
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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