A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949313



Internal ID21369383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149764542..149764542hg38UCSC Ensembl
chr3:149482329..149482329hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191005
SamplesHG002
Known GenesANKUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949313
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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