A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580358



Internal ID16367767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56339632..56358425hg38UCSC Ensembl
Innerchr19:56851001..56869794hg19UCSC Ensembl
Innerchr19:61542813..61561606hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3818794
hg1918794
hg1818794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6584n54
Supporting Variantsnssv901824
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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