A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186397



Internal ID21325214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62105816..62105816hg38UCSC Ensembl
chr20:60680872..60680872hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931823
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186397
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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