A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578314



Internal ID16019037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1622459..1628265hg38UCSC Ensembl
Innerchr19:1622458..1628264hg19UCSC Ensembl
Innerchr19:1573458..1579264hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385807
hg195807
hg185807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6205n54
Supporting Variantsnssv891841
Samples
Known GenesTCF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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