A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578330



Internal ID16365739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1627846..1630342hg38UCSC Ensembl
Innerchr19:1627845..1630341hg19UCSC Ensembl
Innerchr19:1578845..1581341hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382497
hg192497
hg182497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891935
Samples
Known GenesTCF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578330
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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