A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560646



Internal ID22429441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23700232..23700232hg38UCSC Ensembl
chr14:24169441..24169441hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372560, nssv14372561
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560646
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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