A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146011



Internal ID18851700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:11399..68808hg38UCSC Ensembl
Outerchr4:11399..68700hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3857410
hg1957302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997376
SamplesKWB1
Known GenesZNF595, ZNF718
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146011
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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