A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155552



Internal ID22086057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10066953..10074331hg38UCSC Ensembl
Outerchr19:10065948..10080509hg38UCSC Ensembl
Innerchr19:10177629..10185007hg19UCSC Ensembl
Outerchr19:10176624..10191185hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3814562
hg1914562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013453
Samples
Known GenesC3P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155552
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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