A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579391



Internal ID16020114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268140..35270013hg38UCSC Ensembl
Innerchr19:35759043..35760916hg19UCSC Ensembl
Innerchr19:40450883..40452756hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381874
hg191874
hg181874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6416n54
Supporting Variantsnssv898771
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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