A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762358



Internal ID18967772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15271876..15271962hg38UCSC Ensembl
Outerchr19:15382687..15382773hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078911
Supporting Variants
SamplesKWP1
Known GenesBRD4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762358
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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