A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877669



Internal ID16171625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295482..5296297hg38UCSC Ensembl
Innerchr18:5295481..5296296hg19UCSC Ensembl
Innerchr18:5285481..5286296hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38816
hg19816
hg18816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576358
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)nssv877669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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