A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578270



Internal ID16018993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1222613..1244776hg38UCSC Ensembl
Innerchr19:1222612..1244775hg19UCSC Ensembl
Innerchr19:1173612..1195775hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3822164
hg1922164
hg1822164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6196n54
Supporting Variantsnssv891772, nssv891773
Samples
Known GenesATP5D, C19orf26, STK11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578270
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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