A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578362



Internal ID16365771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1950567..1951552hg38UCSC Ensembl
Innerchr19:1950566..1951551hg19UCSC Ensembl
Innerchr19:1901566..1902551hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38986
hg19986
hg18986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6213n54
Supporting Variantsnssv892037, nssv892039, nssv892038, nssv892036, nssv892040
Samples
Known GenesCSNK1G2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578362
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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