A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576860



Internal ID16364269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:49061284..49124067hg38UCSC Ensembl
Innerchr18:46587654..46650437hg19UCSC Ensembl
Innerchr18:44841652..44904435hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3862784
hg1962784
hg1862784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150253
SamplesNINDS_119
Known GenesDYM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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