A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187777



Internal ID21326609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31689270..31689270hg38UCSC Ensembl
chr20:30277073..30277073hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937069
Supporting Variants
SamplesHG002
Known GenesBCL2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187777
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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