A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576351



Internal ID16363760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295349..5295812hg38UCSC Ensembl
Innerchr18:5295348..5295811hg19UCSC Ensembl
Innerchr18:5285348..5285811hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38464
hg19464
hg18464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877649
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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