A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578535



Internal ID16019258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7693308..7695738hg38UCSC Ensembl
Innerchr19:7758194..7760624hg19UCSC Ensembl
Innerchr19:7664194..7666624hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382431
hg192431
hg182431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893300
Samples
Known GenesFCER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578535
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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