A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149422



Internal ID19199616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63200157..63200230hg38UCSC Ensembl
Outerchr20:61831509..61831582hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000724
SamplesKWB1
Known GenesYTHDF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149422
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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