A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576362



Internal ID16363771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295482..5298760hg38UCSC Ensembl
Innerchr18:5295481..5298759hg19UCSC Ensembl
Innerchr18:5285481..5288759hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383279
hg193279
hg183279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877675
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576362
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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