A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950579



Internal ID21370649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32366523..32366523hg38UCSC Ensembl
chr11:32388069..32388069hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192680
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950579
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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