A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150593



Internal ID15876735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40335688..40361542hg38UCSC Ensembl
Innerchr18:37915652..37941506hg19UCSC Ensembl
Innerchr18:36169650..36195504hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3825855
hg1925855
hg1825855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576672
Supporting Variants
SamplesHGDP00886
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150593
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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