A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190792



Internal ID21329650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10802029..10802029hg38UCSC Ensembl
chr11:10823576..10823576hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950857
Supporting Variants
SamplesHG002
Known GenesEIF4G2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190792
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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