A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576355



Internal ID16363764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295349..5296461hg38UCSC Ensembl
Innerchr18:5295348..5296460hg19UCSC Ensembl
Innerchr18:5285348..5286460hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381113
hg191113
hg181113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5829n54
Supporting Variantsnssv877659, nssv877660
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576355
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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