A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893209



Internal ID15840479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6969846..7018858hg38UCSC Ensembl
Innerchr19:6969857..7018869hg19UCSC Ensembl
Innerchr19:6920857..6969869hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3849013
hg1949013
hg1849013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578480
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)nssv893209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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