A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984179



Internal ID18891344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90841781..90841846hg38UCSC Ensembl
Outerchr9:93604063..93604128hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125970
Supporting Variants
SamplesKWS2
Known GenesSYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984179
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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