A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576600



Internal ID16364009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29843410..30617552hg38UCSC Ensembl
Innerchr18:27423375..28197518hg19UCSC Ensembl
Innerchr18:25677373..26451516hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38774143
hg19774144
hg18774144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149711
SamplesHGDP00707
Known GenesMIR302F
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576600
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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