A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525909



Internal ID22395287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10274673..10274759hg38UCSC Ensembl
chr1:10334731..10334817hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325003, nssv14325004, nssv14325005, nssv14325002, nssv14325006
SamplesHG00512, NA19238, NA19239, HG00513, HG00514
Known GenesKIF1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525909
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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