A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987980



Internal ID18867973
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 StatusS
Merged Variantsnsv1133144
Supporting Variants
SamplesKWS1
Known GenesGTPBP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987980
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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