A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133144



Internal ID18906072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1011391..1011493hg38UCSC Ensembl
Outerchr10:1057331..1057433hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987980
SamplesKWS1
Known GenesGTPBP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133144
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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