A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945757



Internal ID21365826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71387784..71387784hg38UCSC Ensembl
chr11:71098830..71098830hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192730
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945757
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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