A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966921



Internal ID18893401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90841972..90842120hg38UCSC Ensembl
Outerchr9:93604254..93604402hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130609
Supporting Variants
SamplesKWS2
Known GenesSYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966921
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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