A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998250



Internal ID19192582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64327900..64332201hg38UCSC Ensembl
Outerchr15:64620099..64624400hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384302
hg194302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146885
Supporting Variants
SamplesKWB1
Known GenesCSNK1G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998250
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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