A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576810



Internal ID16364219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:45725820..45727588hg38UCSC Ensembl
Innerchr18:43305785..43307553hg19UCSC Ensembl
Innerchr18:41559783..41561551hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381769
hg191769
hg181769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv882694
Samples
Known GenesSLC14A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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