A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576359



Internal ID16363768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295482..5296401hg38UCSC Ensembl
Innerchr18:5295481..5296400hg19UCSC Ensembl
Innerchr18:5285481..5286400hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38920
hg19920
hg18920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5830n54
Supporting Variantsnssv877672, nssv877670, nssv877671
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576359
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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