A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954256



Internal ID21374186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62784008..62784008hg38UCSC Ensembl
chr11:62551480..62551480hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191450
SamplesHG002
Known GenesTAF6L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954256
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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