A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001897



Internal ID19191112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1277255..1278356hg38UCSC Ensembl
Outerchr20:1257899..1259000hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150964
Supporting Variants
SamplesKWB1
Known GenesSNPH
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001897
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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