A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190911



Internal ID21329778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67222609..67222609hg38UCSC Ensembl
chr11:66990080..66990080hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932343
Supporting Variants
SamplesHG002
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190911
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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