A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877611



Internal ID16171567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5294903..5296401hg38UCSC Ensembl
Innerchr18:5294902..5296400hg19UCSC Ensembl
Innerchr18:5284902..5286400hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576340
Supporting Variants
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877611
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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