A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578271



Internal ID16018994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1226005..1244901hg38UCSC Ensembl
Innerchr19:1226004..1244900hg19UCSC Ensembl
Innerchr19:1177004..1195900hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3818897
hg1918897
hg1818897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6196n54
Supporting Variantsnssv891774
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)nsv578271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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