A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562763



Internal ID22431509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194311184..194311184hg38UCSC Ensembl
chr3:194028973..194028973hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310279, nssv14310280
SamplesNA19238, NA19239
Known GenesLINC00887
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562763
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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