A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv882630



Internal ID16176586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:45089622..45138039hg38UCSC Ensembl
Innerchr18:42669587..42718004hg19UCSC Ensembl
Innerchr18:40923585..40972002hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3848418
hg1948418
hg1848418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576803
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv882630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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