A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929352



Internal ID21349422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3820807..3820915hg38UCSC Ensembl
chr19:3820805..3820913hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177318
SamplesHG002
Known GenesZFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929352
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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