A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928459



Internal ID21348528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10293157..10293157hg38UCSC Ensembl
chr12:10445756..10445756hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192406
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928459
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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