A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150494



Internal ID18849158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46615117..46644318hg38UCSC Ensembl
Outerchr10:46905299..46934500hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3829202
hg1929202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003793
SamplesKWB1
Known GenesFAM35BP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150494
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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