A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579347



Internal ID16020070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34480941..34482043hg38UCSC Ensembl
Innerchr19:34971846..34972948hg19UCSC Ensembl
Innerchr19:39663686..39664788hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381103
hg191103
hg181103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898577
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579347
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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