A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954212



Internal ID21374282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66431845..66431845hg38UCSC Ensembl
chr2:66658977..66658977hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187176
SamplesHG002
Known GenesMEIS1-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954212
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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