A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569027



Internal ID18520622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:136228..249310hg38UCSC Ensembl
Innerchr18:136228..249310hg19UCSC Ensembl
Innerchr18:126228..239310hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38113083
hg19113083
hg18113083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066441
Supporting Variants
Samples
Known GenesTHOC1, USP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569027
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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