A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576354



Internal ID16363763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295349..5296401hg38UCSC Ensembl
Innerchr18:5295348..5296400hg19UCSC Ensembl
Innerchr18:5285348..5286400hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381053
hg191053
hg181053
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5828n54
Supporting Variantsnssv877657, nssv877656, nssv877654, nssv877658, nssv877655
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576354
Frequency
Sample Size17421
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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