A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996229



Internal ID18840963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63780365..63844266hg38UCSC Ensembl
Outerchr9:68376099..68440000hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3863902
hg1963902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150753
Supporting Variants
SamplesKWB1
Known GenesLOC642236
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996229
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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