A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960233



Internal ID19222424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:119169422..119172622hg38UCSC Ensembl
Outerchr9:121931700..121934900hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110579
Supporting Variants
SamplesKWS1
Known GenesBRINP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960233
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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