A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899272



Internal ID16193228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39894848..39895316hg38UCSC Ensembl
Innerchr19:40385488..40385956hg19UCSC Ensembl
Innerchr19:45077328..45077796hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38469
hg19469
hg18469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579519
Supporting Variants
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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