A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220261



Internal ID22365012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33681884..33681937hg38UCSC Ensembl
chr14:34151090..34151143hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370866
SamplesNA19240
Known GenesNPAS3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220261
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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