A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000071



Internal ID19192599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:67112354..67113281hg38UCSC Ensembl
Outerchr15:67404692..67405619hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147295
Supporting Variants
SamplesKWB1
Known GenesSMAD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000071
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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