A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960183



Internal ID19219300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40321082..40358882hg38UCSC Ensembl
Outerchr9:42466100..42503900hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3837801
hg1937801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110530
Supporting Variants
SamplesKWS1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960183
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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