A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186428



Internal ID21325245
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937128
Supporting Variants
SamplesHG002
Known GenesSTMN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186428
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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