A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578353



Internal ID16365762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1950504..1951496hg38UCSC Ensembl
Innerchr19:1950503..1951495hg19UCSC Ensembl
Innerchr19:1901503..1902495hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38993
hg19993
hg18993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6213n54
Supporting Variantsnssv892003, nssv892002
Samples
Known GenesCSNK1G2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578353
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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