A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192834



Internal ID21331702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126473080..126473080hg38UCSC Ensembl
chr11:126342975..126342975hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928669
Supporting Variants
SamplesHG002
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192834
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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