A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996354



Internal ID18844133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131939061..131939612hg38UCSC Ensembl
Outerchr10:133752565..133753116hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147568
Supporting Variants
SamplesKWB1
Known GenesPPP2R2D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996354
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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