A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998612



Internal ID18843870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106935942..106941043hg38UCSC Ensembl
Outerchr4:107857099..107862200hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149823
Supporting Variants
SamplesKWB1
Known GenesDKK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998612
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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