A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953871



Internal ID21373940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61377729..61377729hg38UCSC Ensembl
chr11:61145201..61145201hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191441
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953871
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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