A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762019



Internal ID19312898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29622556..29622617hg38UCSC Ensembl
Outerchr19:30113463..30113524hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078914
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762019
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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