A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150010



Internal ID15855145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:289153..407958hg38UCSC Ensembl
Innerchr18:289153..407958hg19UCSC Ensembl
Innerchr18:279153..397958hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38118806
hg19118806
hg18118806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576235
Supporting Variants
Samples1780862457_A
Known GenesCOLEC12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150010
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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