A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961727



Internal ID18869630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90840918..90842718hg38UCSC Ensembl
Outerchr9:93603200..93605000hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129054
Supporting Variants
SamplesKWS1
Known GenesSYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961727
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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