A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576522



Internal ID16363931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12657540..12658404hg38UCSC Ensembl
Innerchr18:12657539..12658403hg19UCSC Ensembl
Innerchr18:12647539..12648403hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38865
hg19865
hg18865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5864n54
Supporting Variantsnssv878407
Samples
Known GenesSPIRE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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