A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056707



Internal ID18799238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:231508..290812hg38UCSC Ensembl
Innerchr18:231508..290812hg19UCSC Ensembl
Innerchr18:221508..280812hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3859305
hg1959305
hg1859305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3303n100
Supporting Variantsnssv3569030
Samples
Known GenesTHOC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056707
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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