A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578156



Internal ID16365565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:580333..581956hg38UCSC Ensembl
Innerchr19:580333..581956hg19UCSC Ensembl
Innerchr19:531333..532956hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381624
hg191624
hg181624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6175n54
Supporting Variantsnssv891226
Samples
Known GenesBSG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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