A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978289



Internal ID19233817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39807682..39823982hg38UCSC Ensembl
Outerchr9:41952700..41969000hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3816301
hg1916301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139953
Supporting Variants
SamplesKWS2
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978289
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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