A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951240



Internal ID21371309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37914404..37914404hg38UCSC Ensembl
chr20:36542806..36542806hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186368
SamplesHG002
Known GenesVSTM2L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951240
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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