A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576338



Internal ID16017061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5288696..5295535hg38UCSC Ensembl
Innerchr18:5288695..5295534hg19UCSC Ensembl
Innerchr18:5278695..5285534hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386840
hg196840
hg186840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877608
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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