A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578263



Internal ID16018986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137936..1148867hg38UCSC Ensembl
Innerchr19:1137935..1148866hg19UCSC Ensembl
Innerchr19:1088935..1099866hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810932
hg1910932
hg1810932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6195n54
Supporting Variantsnssv891765
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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