A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578349



Internal ID16365758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1950504..1951124hg38UCSC Ensembl
Innerchr19:1950503..1951123hg19UCSC Ensembl
Innerchr19:1901503..1902123hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38621
hg19621
hg18621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6212n54
Supporting Variantsnssv891982, nssv891971, nssv891974, nssv891967, nssv891985, nssv891970, nssv891972, nssv891977, nssv891968, nssv891973, nssv891975, nssv891979, nssv891980, nssv891983, nssv891981, nssv891984, nssv891976, nssv891978, nssv891966, nssv891969
Samples
Known GenesCSNK1G2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578349
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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