A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988432



Internal ID18865571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90884250..90884350hg38UCSC Ensembl
Outerchr9:93646532..93646632hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134926
Supporting Variants
SamplesKWS1
Known GenesSYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988432
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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