A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561284



Internal ID22430066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12025039..12025039hg38UCSC Ensembl
chr1:12085096..12085096hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330349, nssv14330348
SamplesNA19238, NA19239
Known GenesMIIP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561284
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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