A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529453



Internal ID22398845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101819584..101819654hg38UCSC Ensembl
chr10:103579341..103579411hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352980
SamplesNA19238
Known GenesKCNIP2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529453
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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