A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966923



Internal ID19244949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:109667920..109668235hg38UCSC Ensembl
Outerchr9:112430200..112430515hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112200
Supporting Variants
SamplesKWS2
Known GenesPALM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966923
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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