A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937128



Internal ID21357197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63642015..63642015hg38UCSC Ensembl
chr20:62273368..62273368hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186428
SamplesHG002
Known GenesSTMN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937128
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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