A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954668



Internal ID17303541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:31586453..31586564hg38UCSC Ensembl
Outerchr19:32077359..32077470hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002922
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954668
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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