A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4000n106



Internal ID22797828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39807682..39823982hg38UCSC Ensembl
chr9:41952700..41969000hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3816301
hg1916301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110524, nsv1139953
SamplesKWS2, KWS1
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4000n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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