A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948275



Internal ID21368344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36287072..36287072hg38UCSC Ensembl
chr11:36308622..36308622hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190844
SamplesHG002
Known GenesCOMMD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948275
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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