A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578268



Internal ID16018991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1221162..1250886hg38UCSC Ensembl
Innerchr19:1221161..1250885hg19UCSC Ensembl
Innerchr19:1172161..1201885hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3829725
hg1929725
hg1829725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891770
Samples
Known GenesATP5D, C19orf26, MIDN, STK11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578268
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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