A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877655



Internal ID16171611
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576354
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)nssv877655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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