A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959755



Internal ID19223056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123903821..123907221hg38UCSC Ensembl
Outerchr9:126666100..126669500hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383401
hg193401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119317
Supporting Variants
SamplesKWS1
Known GenesDENND1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959755
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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