A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578162



Internal ID16018885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:583460..593319hg38UCSC Ensembl
Innerchr19:583460..593319hg19UCSC Ensembl
Innerchr19:534460..544319hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389860
hg199860
hg189860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6174n54
Supporting Variantsnssv891232
Samples
Known GenesBSG, HCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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