A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932492



Internal ID21352561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98837542..98837718hg38UCSC Ensembl
chr3:98556386..98556562hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180412
SamplesHG002
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932492
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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