A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529300



Internal ID22398693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35150828..35150893hg38UCSC Ensembl
chr10:35439756..35439821hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340865, nssv14340869, nssv14340866, nssv14340868, nssv14340864, nssv14340867
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00733
Known GenesCREM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529300
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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