A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561204



Internal ID22428715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30462752..30462752hg38UCSC Ensembl
chr19:30953659..30953659hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285868, nssv14285867
SamplesNA19238, NA19240
Known GenesZNF536
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561204
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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