A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578452



Internal ID16019175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4674787..4774202hg38UCSC Ensembl
Innerchr19:4674799..4774214hg19UCSC Ensembl
Innerchr19:4625799..4725214hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3899416
hg1999416
hg1899416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv892933
Samples
Known GenesDPP9, LOC100131094, MIR7-3, MIR7-3HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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