A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934702



Internal ID21354772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37540541..37540541hg38UCSC Ensembl
chr19:38031443..38031443hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186899
SamplesHG002
Known GenesZNF793
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934702
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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