A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075361



Internal ID18978808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1640038..1647500hg38UCSC Ensembl
chr1:1575399..1584500hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg387463
hg199102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762885
SamplesKWP1
Known GenesCDK11B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075361
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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