A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929477



Internal ID21349547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98930326..98930326hg38UCSC Ensembl
chr2:99546789..99546789hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187194
SamplesHG002
Known GenesKIAA1211L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929477
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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