A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893199



Internal ID15840469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6957866..7018169hg38UCSC Ensembl
Innerchr19:6957877..7018180hg19UCSC Ensembl
Innerchr19:6908877..6969180hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3860304
hg1960304
hg1860304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578475
Supporting Variants
Samples
Known GenesEMR4P, FLJ25758
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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