A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148337



Internal ID19201724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:67387541..67389742hg38UCSC Ensembl
Outerchr10:69147299..69149500hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000376
SamplesKWB1
Known GenesCTNNA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148337
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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