A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930996



Internal ID21351065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65166588..65166588hg38UCSC Ensembl
chr2:65393722..65393722hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187170
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930996
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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