A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931296



Internal ID21351365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100451756..100451756hg38UCSC Ensembl
chr3:100170600..100170600hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189838
SamplesHG002
Known GenesLNP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931296
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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