A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963860



Internal ID18878052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:8905210..8905290hg38UCSC Ensembl
Outerchr17:8808527..8808607hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129589
Supporting Variants
SamplesKWS1
Known GenesPIK3R5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963860
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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