A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951852



Internal ID21371921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31004648..31004768hg38UCSC Ensembl
chr19:31495554..31495674hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177610
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951852
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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