A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576444



Internal ID16363853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9205481..9206604hg38UCSC Ensembl
Innerchr18:9205479..9206602hg19UCSC Ensembl
Innerchr18:9195479..9196602hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381124
hg191124
hg181124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5848n54
Supporting Variantsnssv878055
Samples
Known GenesANKRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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