A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192260



Internal ID21331131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68372443..68372443hg38UCSC Ensembl
chr11:68139911..68139911hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951472
Supporting Variants
SamplesHG002
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192260
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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