A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125970



Internal ID18911597
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 StatusM
Merged Variants
Supporting Variantsnssv3984179
SamplesKWS2
Known GenesSYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125970
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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