A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899385



Internal ID16193341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39896716..39902512hg38UCSC Ensembl
Innerchr19:40387356..40392585hg19UCSC Ensembl
Innerchr19:45079196..45084425hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385797
hg195230
hg185230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579523
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)nssv899385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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