A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579389



Internal ID16020112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268140..35269510hg38UCSC Ensembl
Innerchr19:35759043..35760413hg19UCSC Ensembl
Innerchr19:40450883..40452253hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381371
hg191371
hg181371
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898768, nssv898769, nssv898767
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579389
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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