A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578225



Internal ID16018948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137305..1137997hg38UCSC Ensembl
Innerchr19:1137304..1137996hg19UCSC Ensembl
Innerchr19:1088304..1088996hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38693
hg19693
hg18693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6188n54
Supporting Variantsnssv891609, nssv891608
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578225
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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