A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578307



Internal ID16365716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566611..1567450hg38UCSC Ensembl
Innerchr19:1566610..1567449hg19UCSC Ensembl
Innerchr19:1517610..1518449hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6202n54
Supporting Variantsnssv891831, nssv891829, nssv891830
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578307
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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