A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222150



Internal ID22366317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32913901..32916350hg38UCSC Ensembl
chr10:33202829..33205278hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382450
hg192450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338108
SamplesHG00731
Known GenesITGB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222150
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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