A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001892



Internal ID19192672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:50205060..50205176hg38UCSC Ensembl
Outerchr22:50643489..50643605hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150959
Supporting Variants
SamplesKWB1
Known GenesSELO
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001892
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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