A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878403



Internal ID16172359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12657321..12658404hg38UCSC Ensembl
Innerchr18:12657320..12658403hg19UCSC Ensembl
Innerchr18:12647320..12648403hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381084
hg191084
hg181084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576519
Supporting Variants
Samples
Known GenesSPIRE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878403
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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